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rs148158093

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs148158093(A;A)
Make rs148158093(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position101403828
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs148158093
ebirs148158093
HLIrs148158093
Exacrs148158093
Varsomers148158093
Maprs148158093
PheGenIrs148158093
hapmaprs148158093
1000 genomesrs148158093
hgdprs148158093
ensemblrs148158093
gopubmedrs148158093
geneviewrs148158093
scholarrs148158093
googlers148158093
pharmgkbrs148158093
gwascentralrs148158093
openSNPrs148158093
23andMers148158093
23andMe allrs148158093
SNP Nexus

SNPshotrs148158093
SNPdbers148158093
MSV3drs148158093
GWAS Ctlgrs148158093
Max Magnitude0
ClinVar
Risk rs148158093(A;A)
Alt rs148158093(A;A)
Reference rs148158093(G;G)
Significance Probable-Pathogenic
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 RCV000035303.5, RCV000078277.6,