rs201239579
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs201239579(G;T) |
Make rs201239579(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 4 |
Position | 6302049 |
Gene | WFS1 |
is a | snp |
is | mentioned by |
dbSNP | rs201239579 |
dbSNP (classic) | rs201239579 |
ClinGen | rs201239579 |
ebi | rs201239579 |
HLI | rs201239579 |
Exac | rs201239579 |
Gnomad | rs201239579 |
Varsome | rs201239579 |
LitVar | rs201239579 |
Map | rs201239579 |
PheGenI | rs201239579 |
Biobank | rs201239579 |
1000 genomes | rs201239579 |
hgdp | rs201239579 |
ensembl | rs201239579 |
geneview | rs201239579 |
scholar | rs201239579 |
rs201239579 | |
pharmgkb | rs201239579 |
gwascentral | rs201239579 |
openSNP | rs201239579 |
23andMe | rs201239579 |
SNPshot | rs201239579 |
SNPdbe | rs201239579 |
MSV3d | rs201239579 |
GWAS Ctlg | rs201239579 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs201239579(T;T) |
Alt | rs201239579(T;T) |
Reference | Rs201239579(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | WFS1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000004.11:g.6303776G>T |
CLNSRC | |
CLNACC | RCV000195490.2, |