Variant report

Variant	esv3482036
Chromosome Location	chr9:16905593-16905932
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 27 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:27 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112883542	chr9:16905603-16905604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs558504206	chr9:16905606-16905607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs10810662	chr9:16905615-16905616	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs372439794	chr9:16905616-16905617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs5896721	chr9:16905621-16905622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs531505900	chr9:16905624-16905625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs200458495	chr9:16905625-16905626	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs11299500	chr9:16905629-16905630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs5896722	chr9:16905630-16905631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs200422847	chr9:16905686-16905687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs566998879	chr9:16905689-16905690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs529670491	chr9:16905728-16905729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs376112656	chr9:16905780-16905781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs201450612	chr9:16905785-16905786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192864759	chr9:16905806-16905807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs10962680	chr9:16905824-16905825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs10962681	chr9:16905827-16905828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs368186119	chr9:16905834-16905835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs546657905	chr9:16905839-16905840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568225194	chr9:16905844-16905845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs544941718	chr9:16905845-16905846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs535412622	chr9:16905865-16905866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs377030810	chr9:16905866-16905867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs556983023	chr9:16905890-16905891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569915931	chr9:16905900-16905901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs536973358	chr9:16905902-16905903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs118186507	chr9:16905916-16905917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Glioblastoma multiforme	18628472	CNVD
Breast cancer	21611746	CNVD
Breast cancer	21364760	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16902000-16914800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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