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rs869312158

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869312158(G;G)
Make rs869312158(G;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101398419
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs869312158
ebirs869312158
HLIrs869312158
Exacrs869312158
Varsomers869312158
Maprs869312158
PheGenIrs869312158
hapmaprs869312158
1000 genomesrs869312158
hgdprs869312158
ensemblrs869312158
gopubmedrs869312158
geneviewrs869312158
scholarrs869312158
googlers869312158
pharmgkbrs869312158
gwascentralrs869312158
openSNPrs869312158
23andMers869312158
23andMe allrs869312158
SNP Nexus

SNPshotrs869312158
SNPdbers869312158
MSV3drs869312158
GWAS Ctlgrs869312158
Max Magnitude0
ClinVar
Risk rs869312158(G;G)
Alt rs869312158(G;G)
Reference rs869312158(T;T)
Significance Drug-response
Disease Fabry disease Deoxygalactonojirimycin response
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry disease Deoxygalactonojirimycin response
Reversed 1
HGVS NC_000023.10:g.100653407A>C
CLNSRC
CLNACC RCV000209347.1, RCV000209621.1,