rs35769976
From SNPedia
					| Orientation | plus | 
| Stabilized | plus | 
| Geno | Mag | Summary | 
|---|---|---|
| (C;C) | 0 | common in complete genomics | 
| (G;G) | 0 | common in clinvar | 
| Make rs35769976(C;G) | 
| Reference | GRCh38 38.1/141 | 
| Chromosome | 19 | 
| Position | 15180765 | 
| Gene | MIR6795, NOTCH3 | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs35769976 | 
| dbSNP (classic) | rs35769976 | 
| ClinGen | rs35769976 | 
| ebi | rs35769976 | 
| HLI | rs35769976 | 
| Exac | rs35769976 | 
| Gnomad | rs35769976 | 
| Varsome | rs35769976 | 
| LitVar | rs35769976 | 
| Map | rs35769976 | 
| PheGenI | rs35769976 | 
| Biobank | rs35769976 | 
| 1000 genomes | rs35769976 | 
| hgdp | rs35769976 | 
| ensembl | rs35769976 | 
| geneview | rs35769976 | 
| scholar | rs35769976 | 
| rs35769976 | |
| pharmgkb | rs35769976 | 
| gwascentral | rs35769976 | 
| openSNP | rs35769976 | 
| 23andMe | rs35769976 | 
| SNPshot | rs35769976 | 
| SNPdbe | rs35769976 | 
| MSV3d | rs35769976 | 
| GWAS Ctlg | rs35769976 | 
| GMAF | 0.08356 | 
| Max Magnitude | 0 | 
| ClinVar | |
|---|---|
| Risk | rs35769976(A;A) Rs35769976(G;G) rs35769976(T;T) | 
| Alt | rs35769976(A;A) Rs35769976(G;G) rs35769976(T;T) | 
| Reference | Rs35769976(C;C) | 
| Significance | Other | 
| Disease | Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy not specified | 
| Variation | info | 
| Gene | NOTCH3 MIR6795 | 
| CLNDBN | Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy not specified | 
| Reversed | 0 | 
| HGVS | NC_000019.9:g.15291576C>G | 
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) | 
| CLNACC | RCV000009808.4, RCV000243215.1, | 
