rs150382575
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs150382575(A;A) |
Make rs150382575(A;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 12 |
Position | 21574248 |
Gene | GYS2 |
is a | snp |
is | mentioned by |
dbSNP | rs150382575 |
dbSNP (classic) | rs150382575 |
ClinGen | rs150382575 |
ebi | rs150382575 |
HLI | rs150382575 |
Exac | rs150382575 |
Gnomad | rs150382575 |
Varsome | rs150382575 |
LitVar | rs150382575 |
Map | rs150382575 |
PheGenI | rs150382575 |
Biobank | rs150382575 |
1000 genomes | rs150382575 |
hgdp | rs150382575 |
ensembl | rs150382575 |
geneview | rs150382575 |
scholar | rs150382575 |
rs150382575 | |
pharmgkb | rs150382575 |
gwascentral | rs150382575 |
openSNP | rs150382575 |
23andMe | rs150382575 |
SNPshot | rs150382575 |
SNPdbe | rs150382575 |
MSV3d | rs150382575 |
GWAS Ctlg | rs150382575 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs150382575(A;A) rs150382575(T;T) |
Alt | rs150382575(A;A) rs150382575(T;T) |
Reference | Rs150382575(G;G) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | GYS2 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000012.11:g.21727182G>A |
CLNSRC | |
CLNACC | RCV000196241.1, |