rs769688376
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs769688376(A;A) |
Make rs769688376(A;C) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 19 |
Position | 36089289 |
Gene | WDR62 |
is a | snp |
is | mentioned by |
dbSNP | rs769688376 |
dbSNP (classic) | rs769688376 |
ClinGen | rs769688376 |
ebi | rs769688376 |
HLI | rs769688376 |
Exac | rs769688376 |
Gnomad | rs769688376 |
Varsome | rs769688376 |
LitVar | rs769688376 |
Map | rs769688376 |
PheGenI | rs769688376 |
Biobank | rs769688376 |
1000 genomes | rs769688376 |
hgdp | rs769688376 |
ensembl | rs769688376 |
geneview | rs769688376 |
scholar | rs769688376 |
rs769688376 | |
pharmgkb | rs769688376 |
gwascentral | rs769688376 |
openSNP | rs769688376 |
23andMe | rs769688376 |
SNPshot | rs769688376 |
SNPdbe | rs769688376 |
MSV3d | rs769688376 |
GWAS Ctlg | rs769688376 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs769688376(A;A) |
Alt | rs769688376(A;A) |
Reference | Rs769688376(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | WDR62 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000019.9:g.36580191C>A |
CLNSRC | |
CLNACC | RCV000330039.1, |