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rs869312165

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312165(G;T)
Make rs869312165(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101397923
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs869312165
ebirs869312165
HLIrs869312165
Exacrs869312165
Varsomers869312165
Maprs869312165
PheGenIrs869312165
hapmaprs869312165
1000 genomesrs869312165
hgdprs869312165
ensemblrs869312165
gopubmedrs869312165
geneviewrs869312165
scholarrs869312165
googlers869312165
pharmgkbrs869312165
gwascentralrs869312165
openSNPrs869312165
23andMers869312165
23andMe allrs869312165
SNP Nexus

SNPshotrs869312165
SNPdbers869312165
MSV3drs869312165
GWAS Ctlgrs869312165
Max Magnitude0
ClinVar
Risk rs869312165(T;T)
Alt rs869312165(T;T)
Reference rs869312165(G;G)
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.100652911C>A
CLNSRC
CLNACC RCV000208905.1, RCV000209170.1,