rs776814755
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs776814755(C;T) |
Make rs776814755(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 15 |
Position | 27851390 |
Gene | OCA2 |
is a | snp |
is | mentioned by |
dbSNP | rs776814755 |
dbSNP (classic) | rs776814755 |
ClinGen | rs776814755 |
ebi | rs776814755 |
HLI | rs776814755 |
Exac | rs776814755 |
Gnomad | rs776814755 |
Varsome | rs776814755 |
LitVar | rs776814755 |
Map | rs776814755 |
PheGenI | rs776814755 |
Biobank | rs776814755 |
1000 genomes | rs776814755 |
hgdp | rs776814755 |
ensembl | rs776814755 |
geneview | rs776814755 |
scholar | rs776814755 |
rs776814755 | |
pharmgkb | rs776814755 |
gwascentral | rs776814755 |
openSNP | rs776814755 |
23andMe | rs776814755 |
SNPshot | rs776814755 |
SNPdbe | rs776814755 |
MSV3d | rs776814755 |
GWAS Ctlg | rs776814755 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs776814755(T;T) |
Alt | rs776814755(T;T) |
Reference | Rs776814755(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | OCA2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000015.9:g.28096536C>T |
CLNSRC | |
CLNACC | RCV000493655.1, |