rs137852343
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 5 | G6PD deficiency |
(C;T) | 3 | Carrier of G6PD deficiency mutation; variable expressivity |
(T;T) | 0 | common in clinvar |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 154534465 |
Gene | G6PD |
is a | snp |
is | mentioned by |
dbSNP | rs137852343 |
dbSNP (classic) | rs137852343 |
ClinGen | rs137852343 |
ebi | rs137852343 |
HLI | rs137852343 |
Exac | rs137852343 |
Gnomad | rs137852343 |
Varsome | rs137852343 |
LitVar | rs137852343 |
Map | rs137852343 |
PheGenI | rs137852343 |
Biobank | rs137852343 |
1000 genomes | rs137852343 |
hgdp | rs137852343 |
ensembl | rs137852343 |
geneview | rs137852343 |
scholar | rs137852343 |
rs137852343 | |
pharmgkb | rs137852343 |
gwascentral | rs137852343 |
openSNP | rs137852343 |
23andMe | rs137852343 |
SNPshot | rs137852343 |
SNPdbe | rs137852343 |
MSV3d | rs137852343 |
GWAS Ctlg | rs137852343 |
Max Magnitude | 5 |
23andMe name: i5008456
ClinVar | |
---|---|
Risk | Rs137852343(C;C) |
Alt | Rs137852343(C;C) |
Reference | Rs137852343(T;T) |
Significance | Other |
Disease | G6PD NANKANG |
Variation | info |
Gene | G6PD |
CLNDBN | G6PD NANKANG |
Reversed | 1 |
HGVS | NC_000023.10:g.153762680A>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000011150.1, |