rs1057524572
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs1057524572(C;G) |
Make rs1057524572(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 9 |
Position | 34647538 |
Gene | GALT |
is a | snp |
is | mentioned by |
dbSNP | rs1057524572 |
dbSNP (classic) | rs1057524572 |
ClinGen | rs1057524572 |
ebi | rs1057524572 |
HLI | rs1057524572 |
Exac | rs1057524572 |
Gnomad | rs1057524572 |
Varsome | rs1057524572 |
LitVar | rs1057524572 |
Map | rs1057524572 |
PheGenI | rs1057524572 |
Biobank | rs1057524572 |
1000 genomes | rs1057524572 |
hgdp | rs1057524572 |
ensembl | rs1057524572 |
geneview | rs1057524572 |
scholar | rs1057524572 |
rs1057524572 | |
pharmgkb | rs1057524572 |
gwascentral | rs1057524572 |
openSNP | rs1057524572 |
23andMe | rs1057524572 |
SNPshot | rs1057524572 |
SNPdbe | rs1057524572 |
MSV3d | rs1057524572 |
GWAS Ctlg | rs1057524572 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057524572(G;G) |
Alt | rs1057524572(G;G) |
Reference | Rs1057524572(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | GALT |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000009.11:g.34647535C>G |
CLNSRC | |
CLNACC | RCV000422602.1, |