rs34193178
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs34193178(C;G) |
Make rs34193178(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | X |
Position | 154532945 |
Gene | G6PD |
is a | snp |
is | mentioned by |
dbSNP | rs34193178 |
dbSNP (classic) | rs34193178 |
ClinGen | rs34193178 |
ebi | rs34193178 |
HLI | rs34193178 |
Exac | rs34193178 |
Gnomad | rs34193178 |
Varsome | rs34193178 |
LitVar | rs34193178 |
Map | rs34193178 |
PheGenI | rs34193178 |
Biobank | rs34193178 |
1000 genomes | rs34193178 |
hgdp | rs34193178 |
ensembl | rs34193178 |
geneview | rs34193178 |
scholar | rs34193178 |
rs34193178 | |
pharmgkb | rs34193178 |
gwascentral | rs34193178 |
openSNP | rs34193178 |
23andMe | rs34193178 |
SNPshot | rs34193178 |
SNPdbe | rs34193178 |
MSV3d | rs34193178 |
GWAS Ctlg | rs34193178 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs34193178(G;G) rs34193178(T;T) |
Alt | rs34193178(G;G) rs34193178(T;T) |
Reference | Rs34193178(C;C) |
Significance | Pathogenic |
Disease | not provided Anemia |
Variation | info |
Gene | G6PD |
CLNDBN | not provided Anemia, nonspherocytic hemolytic, due to G6PD deficiency |
Reversed | 0 |
HGVS | NC_000023.10:g.153761160C>G |
CLNSRC | HGMD |
CLNACC | RCV000079391.3, RCV000180548.1, |