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rs869312159

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312159(C;G)
Make rs869312159(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101398401
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs869312159
ebirs869312159
HLIrs869312159
Exacrs869312159
Varsomers869312159
Maprs869312159
PheGenIrs869312159
hapmaprs869312159
1000 genomesrs869312159
hgdprs869312159
ensemblrs869312159
gopubmedrs869312159
geneviewrs869312159
scholarrs869312159
googlers869312159
pharmgkbrs869312159
gwascentralrs869312159
openSNPrs869312159
23andMers869312159
23andMe allrs869312159
SNP Nexus

SNPshotrs869312159
SNPdbers869312159
MSV3drs869312159
GWAS Ctlgrs869312159
Max Magnitude0
ClinVar
Risk rs869312159(G;G)
Alt rs869312159(G;G)
Reference rs869312159(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.100653389G>C
CLNSRC
CLNACC RCV000209054.1, RCV000209324.1,