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rs869312133

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312133(C;G)
Make rs869312133(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101407897
GeneGLA, HNRNPH2, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs869312133
ebirs869312133
HLIrs869312133
Exacrs869312133
Varsomers869312133
Maprs869312133
PheGenIrs869312133
hapmaprs869312133
1000 genomesrs869312133
hgdprs869312133
ensemblrs869312133
gopubmedrs869312133
geneviewrs869312133
scholarrs869312133
googlers869312133
pharmgkbrs869312133
gwascentralrs869312133
openSNPrs869312133
23andMers869312133
23andMe allrs869312133
SNP Nexus

SNPshotrs869312133
SNPdbers869312133
MSV3drs869312133
GWAS Ctlgrs869312133
Max Magnitude0
ClinVar
Risk rs869312133(G;G)
Alt rs869312133(G;G)
Reference rs869312133(C;C)
Significance Drug-response
Disease Fabry disease Deoxygalactonojirimycin response
Variation info
Gene RPL36A-HNRNPH2 HNRNPH2 GLA
CLNDBN Fabry disease Deoxygalactonojirimycin response
Reversed 1
HGVS NC_000023.10:g.100662885G>C
CLNSRC
CLNACC RCV000209209.1, RCV000209475.1,