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rs113173389

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs113173389(A;A)
Make rs113173389(A;G)
ReferenceGRCh38 38.1/142
ChromosomeX
Position101403899
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs113173389
ebirs113173389
HLIrs113173389
Exacrs113173389
Varsomers113173389
Maprs113173389
PheGenIrs113173389
hapmaprs113173389
1000 genomesrs113173389
hgdprs113173389
ensemblrs113173389
gopubmedrs113173389
geneviewrs113173389
scholarrs113173389
googlers113173389
pharmgkbrs113173389
gwascentralrs113173389
openSNPrs113173389
23andMers113173389
23andMe allrs113173389
SNP Nexus

SNPshotrs113173389
SNPdbers113173389
MSV3drs113173389
GWAS Ctlgrs113173389
Max Magnitude0
ClinVar
Risk rs113173389(A;A)
Alt rs113173389(A;A)
Reference rs113173389(G;G)
Significance Pathogenic
Disease Fabry disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry disease
Reversed 1
HGVS NC_000023.10:g.100658887C>T
CLNSRC HGMD
CLNACC RCV000078274.6,