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rs869312155

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312155(C;T)
Make rs869312155(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101398443
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs869312155
ebirs869312155
HLIrs869312155
Exacrs869312155
Varsomers869312155
Maprs869312155
PheGenIrs869312155
hapmaprs869312155
1000 genomesrs869312155
hgdprs869312155
ensemblrs869312155
gopubmedrs869312155
geneviewrs869312155
scholarrs869312155
googlers869312155
pharmgkbrs869312155
gwascentralrs869312155
openSNPrs869312155
23andMers869312155
23andMe allrs869312155
SNP Nexus

SNPshotrs869312155
SNPdbers869312155
MSV3drs869312155
GWAS Ctlgrs869312155
Max Magnitude0
ClinVar
Risk rs869312155(T;T)
Alt rs869312155(T;T)
Reference rs869312155(C;C)
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.100653431G>A
CLNSRC
CLNACC RCV000209571.1, RCV000209717.1,