rs142668478
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs142668478(A;A) |
Make rs142668478(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 4 |
Position | 6301849 |
Gene | WFS1 |
is a | snp |
is | mentioned by |
dbSNP | rs142668478 |
dbSNP (classic) | rs142668478 |
ClinGen | rs142668478 |
ebi | rs142668478 |
HLI | rs142668478 |
Exac | rs142668478 |
Gnomad | rs142668478 |
Varsome | rs142668478 |
LitVar | rs142668478 |
Map | rs142668478 |
PheGenI | rs142668478 |
Biobank | rs142668478 |
1000 genomes | rs142668478 |
hgdp | rs142668478 |
ensembl | rs142668478 |
geneview | rs142668478 |
scholar | rs142668478 |
rs142668478 | |
pharmgkb | rs142668478 |
gwascentral | rs142668478 |
openSNP | rs142668478 |
23andMe | rs142668478 |
SNPshot | rs142668478 |
SNPdbe | rs142668478 |
MSV3d | rs142668478 |
GWAS Ctlg | rs142668478 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs142668478(A;A) rs142668478(C;C) |
Alt | rs142668478(A;A) rs142668478(C;C) |
Reference | Rs142668478(G;G) |
Significance | Pathogenic |
Disease | not specified WFS1-Related Disorders |
Variation | info |
Gene | WFS1 |
CLNDBN | not specified WFS1-Related Disorders |
Reversed | 0 |
HGVS | NC_000004.11:g.6303576G>A; NC_000004.11:g.6303576G>C |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000198254.3, RCV000038650.2, |