rs200672755
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs200672755(A;A) |
Make rs200672755(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 4 |
Position | 6301815 |
Gene | WFS1 |
is a | snp |
is | mentioned by |
dbSNP | rs200672755 |
dbSNP (classic) | rs200672755 |
ClinGen | rs200672755 |
ebi | rs200672755 |
HLI | rs200672755 |
Exac | rs200672755 |
Gnomad | rs200672755 |
Varsome | rs200672755 |
LitVar | rs200672755 |
Map | rs200672755 |
PheGenI | rs200672755 |
Biobank | rs200672755 |
1000 genomes | rs200672755 |
hgdp | rs200672755 |
ensembl | rs200672755 |
geneview | rs200672755 |
scholar | rs200672755 |
rs200672755 | |
pharmgkb | rs200672755 |
gwascentral | rs200672755 |
openSNP | rs200672755 |
23andMe | rs200672755 |
SNPshot | rs200672755 |
SNPdbe | rs200672755 |
MSV3d | rs200672755 |
GWAS Ctlg | rs200672755 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs200672755(A;A) rs200672755(C;C) |
Alt | rs200672755(A;A) rs200672755(C;C) |
Reference | Rs200672755(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | WFS1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000004.11:g.6303542G>A |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000197395.1, |