rs149013740
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs149013740(A;A) |
Make rs149013740(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 4 |
Position | 6301990 |
Gene | WFS1 |
is a | snp |
is | mentioned by |
dbSNP | rs149013740 |
dbSNP (classic) | rs149013740 |
ClinGen | rs149013740 |
ebi | rs149013740 |
HLI | rs149013740 |
Exac | rs149013740 |
Gnomad | rs149013740 |
Varsome | rs149013740 |
LitVar | rs149013740 |
Map | rs149013740 |
PheGenI | rs149013740 |
Biobank | rs149013740 |
1000 genomes | rs149013740 |
hgdp | rs149013740 |
ensembl | rs149013740 |
geneview | rs149013740 |
scholar | rs149013740 |
rs149013740 | |
pharmgkb | rs149013740 |
gwascentral | rs149013740 |
openSNP | rs149013740 |
23andMe | rs149013740 |
SNPshot | rs149013740 |
SNPdbe | rs149013740 |
MSV3d | rs149013740 |
GWAS Ctlg | rs149013740 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs149013740(A;A) |
Alt | rs149013740(A;A) |
Reference | Rs149013740(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided not specified |
Variation | info |
Gene | WFS1 |
CLNDBN | not provided not specified |
Reversed | 0 |
HGVS | NC_000004.11:g.6303717G>A |
CLNSRC | |
CLNACC | RCV000197209.1, RCV000379222.1, |