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rs869312151

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs869312151(C;G)
Make rs869312151(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101398929
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs869312151
ebirs869312151
HLIrs869312151
Exacrs869312151
Varsomers869312151
Maprs869312151
PheGenIrs869312151
hapmaprs869312151
1000 genomesrs869312151
hgdprs869312151
ensemblrs869312151
gopubmedrs869312151
geneviewrs869312151
scholarrs869312151
googlers869312151
pharmgkbrs869312151
gwascentralrs869312151
openSNPrs869312151
23andMers869312151
23andMe allrs869312151
SNP Nexus

SNPshotrs869312151
SNPdbers869312151
MSV3drs869312151
GWAS Ctlgrs869312151
Max Magnitude0
ClinVar
Risk rs869312151(G;G)
Alt rs869312151(G;G)
Reference rs869312151(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.100653917G>C
CLNSRC
CLNACC RCV000209122.1, RCV000209507.1,