rs71537685
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs71537685(A;A) |
Make rs71537685(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 4 |
Position | 6300657 |
Gene | WFS1 |
is a | snp |
is | mentioned by |
dbSNP | rs71537685 |
dbSNP (classic) | rs71537685 |
ClinGen | rs71537685 |
ebi | rs71537685 |
HLI | rs71537685 |
Exac | rs71537685 |
Gnomad | rs71537685 |
Varsome | rs71537685 |
LitVar | rs71537685 |
Map | rs71537685 |
PheGenI | rs71537685 |
Biobank | rs71537685 |
1000 genomes | rs71537685 |
hgdp | rs71537685 |
ensembl | rs71537685 |
geneview | rs71537685 |
scholar | rs71537685 |
rs71537685 | |
pharmgkb | rs71537685 |
gwascentral | rs71537685 |
openSNP | rs71537685 |
23andMe | rs71537685 |
SNPshot | rs71537685 |
SNPdbe | rs71537685 |
MSV3d | rs71537685 |
GWAS Ctlg | rs71537685 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs71537685(A;A) |
Alt | rs71537685(A;A) |
Reference | Rs71537685(G;G) |
Significance | Probable-Pathogenic |
Disease | not specified |
Variation | info |
Gene | WFS1 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000004.11:g.6302384G>A |
CLNSRC | |
CLNACC | RCV000171514.2, |