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rs869312147

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869312147(A;C)
Make rs869312147(C;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101400717
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs869312147
ebirs869312147
HLIrs869312147
Exacrs869312147
Varsomers869312147
Maprs869312147
PheGenIrs869312147
hapmaprs869312147
1000 genomesrs869312147
hgdprs869312147
ensemblrs869312147
gopubmedrs869312147
geneviewrs869312147
scholarrs869312147
googlers869312147
pharmgkbrs869312147
gwascentralrs869312147
openSNPrs869312147
23andMers869312147
23andMe allrs869312147
SNP Nexus

SNPshotrs869312147
SNPdbers869312147
MSV3drs869312147
GWAS Ctlgrs869312147
Max Magnitude0
ClinVar
Risk rs869312147(C;C)
Alt rs869312147(C;C)
Reference rs869312147(A;A)
Significance Drug-response
Disease Deoxygalactonojirimycin response Fabry disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Deoxygalactonojirimycin response Fabry disease
Reversed 1
HGVS NC_000023.10:g.100655705T>G
CLNSRC
CLNACC RCV000209080.1, RCV000209638.1,