Variant report

Variant	nsv964516
Chromosome Location	chr21:15330176-15330676
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 28 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:28 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200211881	chr21:15330212-15330213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs138908319	chr21:15330214-15330215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs182110267	chr21:15330235-15330236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs143172950	chr21:15330243-15330244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371581381	chr21:15330253-15330254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs374954879	chr21:15330284-15330285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs2822327	chr21:15330329-15330330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs565535327	chr21:15330331-15330332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs368857548	chr21:15330362-15330363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534844951	chr21:15330380-15330381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs554351220	chr21:15330381-15330382	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574448114	chr21:15330382-15330383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs543157676	chr21:15330385-15330386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs556876848	chr21:15330404-15330405	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs576954690	chr21:15330441-15330442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs202035197	chr21:15330456-15330457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs2822328	chr21:15330468-15330469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs186826580	chr21:15330472-15330473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs392812	chr21:15330476-15330477	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs2822329	chr21:15330510-15330511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528683598	chr21:15330515-15330516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs550735585	chr21:15330526-15330527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs542376115	chr21:15330558-15330559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs2822330	chr21:15330568-15330569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs562163563	chr21:15330603-15330604	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs138698312	chr21:15330613-15330614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs550803651	chr21:15330616-15330617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs192895144	chr21:15330621-15330622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Down syndrome	17412756	CNVD
Down syndrome	17576883	CNVD
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Sudden cardiac death	19188705	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	21509527	CNVD
T-cell lymphomas	19863542	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Renal cell carcinoma	19461508	CNVD
Seminomas	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Metanephric adenoma	20802469	CNVD
Neuroblastoma	18923191	CNVD
Prostate cancer	19156837	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	20409316	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
lymphocytic leukemia	21291569	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute myeloid leukemia	21251322	CNVD
abnormal development	18461090	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Melanoma	17363583	CNVD
Breast cancer	22522925	CNVD
Multiple myeloma	17550852	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	18923514	CNVD
Alzheimer''s disease	20877625	CNVD
Follicular lymphoma	20505157	CNVD
Alzheimer''s disease	21956041	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Melanoma	18172304	CNVD
Autism	22958593	CNVD
Schizophrenia	22958593	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:15310400-15347400	Weak transcription	Dnd41	blood

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