rs148158093
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs148158093(A;A) |
Make rs148158093(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 101403828 |
Gene | GLA, RPL36A-HNRNPH2 |
is a | snp |
is | mentioned by |
dbSNP | rs148158093 |
dbSNP (classic) | rs148158093 |
ClinGen | rs148158093 |
ebi | rs148158093 |
HLI | rs148158093 |
Exac | rs148158093 |
Gnomad | rs148158093 |
Varsome | rs148158093 |
LitVar | rs148158093 |
Map | rs148158093 |
PheGenI | rs148158093 |
Biobank | rs148158093 |
1000 genomes | rs148158093 |
hgdp | rs148158093 |
ensembl | rs148158093 |
geneview | rs148158093 |
scholar | rs148158093 |
rs148158093 | |
pharmgkb | rs148158093 |
gwascentral | rs148158093 |
openSNP | rs148158093 |
23andMe | rs148158093 |
SNPshot | rs148158093 |
SNPdbe | rs148158093 |
MSV3d | rs148158093 |
GWAS Ctlg | rs148158093 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs148158093(A;A) |
Alt | rs148158093(A;A) |
Reference | Rs148158093(G;G) |
Significance | Other |
Disease | not specified Fabry disease |
Variation | info |
Gene | RPL36A-HNRNPH2 GLA |
CLNDBN | not specified Fabry disease |
Reversed | 0 |
HGVS | NC_000023.10:g.100658816G>A |
CLNSRC | HGMD |
CLNACC | RCV000035303.6, RCV000078277.6, |