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rs869312162

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312162(C;G)
Make rs869312162(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101398044
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs869312162
ebirs869312162
HLIrs869312162
Exacrs869312162
Varsomers869312162
Maprs869312162
PheGenIrs869312162
hapmaprs869312162
1000 genomesrs869312162
hgdprs869312162
ensemblrs869312162
gopubmedrs869312162
geneviewrs869312162
scholarrs869312162
googlers869312162
pharmgkbrs869312162
gwascentralrs869312162
openSNPrs869312162
23andMers869312162
23andMe allrs869312162
SNP Nexus

SNPshotrs869312162
SNPdbers869312162
MSV3drs869312162
GWAS Ctlgrs869312162
Max Magnitude0
ClinVar
Risk rs869312162(G;G)
Alt rs869312162(G;G)
Reference rs869312162(C;C)
Significance Drug-response
Disease Deoxygalactonojirimycin response Fabry disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Deoxygalactonojirimycin response Fabry disease
Reversed 1
HGVS NC_000023.10:g.100653032G>C
CLNSRC
CLNACC RCV000209219.1, RCV000209785.1,