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rs869312140

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869312140(C;C)
Make rs869312140(C;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101403924
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs869312140
ebirs869312140
HLIrs869312140
Exacrs869312140
Varsomers869312140
Maprs869312140
PheGenIrs869312140
hapmaprs869312140
1000 genomesrs869312140
hgdprs869312140
ensemblrs869312140
gopubmedrs869312140
geneviewrs869312140
scholarrs869312140
googlers869312140
pharmgkbrs869312140
gwascentralrs869312140
openSNPrs869312140
23andMers869312140
23andMe allrs869312140
SNP Nexus

SNPshotrs869312140
SNPdbers869312140
MSV3drs869312140
GWAS Ctlgrs869312140
Max Magnitude0
ClinVar
Risk rs869312140(C;C)
Alt rs869312140(C;C)
Reference rs869312140(T;T)
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.100658912A>G
CLNSRC
CLNACC RCV000209126.1, RCV000209399.1,