Variant report

Variant	esv2755625
Chromosome Location	chr3:115901032-115902901
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 73 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:73 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4296590	chr3:115901032-115901033	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs7639528	chr3:115901044-115901045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs201761706	chr3:115901123-115901124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs566138102	chr3:115901125-115901126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs1461134	chr3:115901137-115901138	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs115059539	chr3:115901170-115901171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs576071296	chr3:115901182-115901183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs537749106	chr3:115901192-115901193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs150740149	chr3:115901223-115901224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs139377574	chr3:115901235-115901236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs370281580	chr3:115901239-115901240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs186891625	chr3:115901268-115901269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs190735175	chr3:115901272-115901273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs1461135	chr3:115901292-115901293	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs545946353	chr3:115901309-115901310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs74419206	chr3:115901315-115901316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs7651707	chr3:115901347-115901348	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs17643182	chr3:115901357-115901358	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs1461136	chr3:115901373-115901374	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs1461137	chr3:115901390-115901391	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs534145448	chr3:115901406-115901407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547951178	chr3:115901430-115901431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs566176371	chr3:115901469-115901470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs75056138	chr3:115901500-115901501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs370320130	chr3:115901513-115901514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs183277914	chr3:115901523-115901524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs187947323	chr3:115901546-115901547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs544248605	chr3:115901554-115901555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs144391317	chr3:115901578-115901579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs555494944	chr3:115901629-115901630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs146649199	chr3:115901634-115901635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs535410053	chr3:115901712-115901713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs553914570	chr3:115901728-115901729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs572309019	chr3:115901732-115901733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs189684401	chr3:115901745-115901746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs182858100	chr3:115901774-115901775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs79357967	chr3:115901820-115901821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs543379760	chr3:115901837-115901838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs373778127	chr3:115901863-115901864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs1461138	chr3:115901908-115901909	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs541401544	chr3:115902005-115902006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs559896234	chr3:115902006-115902007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533306956	chr3:115902065-115902066	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551569821	chr3:115902162-115902163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs569783143	chr3:115902170-115902171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs117205640	chr3:115902187-115902188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs549571672	chr3:115902189-115902190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs549335627	chr3:115902222-115902223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs567584194	chr3:115902223-115902224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs56357456	chr3:115902232-115902233	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:62)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Developmental delay	22180640	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Attention deficit hyperactivity disorder	22180640	CNVD
Ovarian cancer	22174824	CNVD
Ductal carcinoma	22052326	CNVD
Myelofibrosis	22110671	CNVD
Characteristic facial feature	22180640	CNVD
hypoplastic male genitals	22180640	CNVD
postnatal overgrowth	22180640	CNVD
Schizophrenia	23813976	CNVD
lymphocytic leukemia	21291569	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:115898600-115907000	Weak transcription	Colon Smooth Muscle	Colon

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