rs141585847
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs141585847(G;G) |
Make rs141585847(G;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 4 |
Position | 6301111 |
Gene | WFS1 |
is a | snp |
is | mentioned by |
dbSNP | rs141585847 |
dbSNP (classic) | rs141585847 |
ClinGen | rs141585847 |
ebi | rs141585847 |
HLI | rs141585847 |
Exac | rs141585847 |
Gnomad | rs141585847 |
Varsome | rs141585847 |
LitVar | rs141585847 |
Map | rs141585847 |
PheGenI | rs141585847 |
Biobank | rs141585847 |
1000 genomes | rs141585847 |
hgdp | rs141585847 |
ensembl | rs141585847 |
geneview | rs141585847 |
scholar | rs141585847 |
rs141585847 | |
pharmgkb | rs141585847 |
gwascentral | rs141585847 |
openSNP | rs141585847 |
23andMe | rs141585847 |
SNPshot | rs141585847 |
SNPdbe | rs141585847 |
MSV3d | rs141585847 |
GWAS Ctlg | rs141585847 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs141585847(G;G) |
Alt | rs141585847(G;G) |
Reference | Rs141585847(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | WFS1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000004.11:g.6302838T>G |
CLNSRC | |
CLNACC | RCV000199551.1, |