rs776996552
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs776996552(C;T) |
Make rs776996552(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 17 |
Position | 38343441 |
Gene | GPR179 |
is a | snp |
is | mentioned by |
dbSNP | rs776996552 |
dbSNP (classic) | rs776996552 |
ClinGen | rs776996552 |
ebi | rs776996552 |
HLI | rs776996552 |
Exac | rs776996552 |
Gnomad | rs776996552 |
Varsome | rs776996552 |
LitVar | rs776996552 |
Map | rs776996552 |
PheGenI | rs776996552 |
Biobank | rs776996552 |
1000 genomes | rs776996552 |
hgdp | rs776996552 |
ensembl | rs776996552 |
geneview | rs776996552 |
scholar | rs776996552 |
rs776996552 | |
pharmgkb | rs776996552 |
gwascentral | rs776996552 |
openSNP | rs776996552 |
23andMe | rs776996552 |
SNPshot | rs776996552 |
SNPdbe | rs776996552 |
MSV3d | rs776996552 |
GWAS Ctlg | rs776996552 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs776996552(T;T) |
Alt | rs776996552(T;T) |
Reference | Rs776996552(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | GPR179 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.36499324C>T |
CLNSRC | |
CLNACC | RCV000171255.1, |