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rs869312139

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869312139(A;T)
Make rs869312139(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101407714
GeneGLA, HNRNPH2, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs869312139
ebirs869312139
HLIrs869312139
Exacrs869312139
Varsomers869312139
Maprs869312139
PheGenIrs869312139
hapmaprs869312139
1000 genomesrs869312139
hgdprs869312139
ensemblrs869312139
gopubmedrs869312139
geneviewrs869312139
scholarrs869312139
googlers869312139
pharmgkbrs869312139
gwascentralrs869312139
openSNPrs869312139
23andMers869312139
23andMe allrs869312139
SNP Nexus

SNPshotrs869312139
SNPdbers869312139
MSV3drs869312139
GWAS Ctlgrs869312139
Max Magnitude0
ClinVar
Risk rs869312139(T;T)
Alt rs869312139(T;T)
Reference rs869312139(A;A)
Significance Drug-response
Disease Fabry disease Deoxygalactonojirimycin response
Variation info
Gene RPL36A-HNRNPH2 HNRNPH2 GLA
CLNDBN Fabry disease Deoxygalactonojirimycin response
Reversed 1
HGVS NC_000023.10:g.100662702T>A
CLNSRC
CLNACC RCV000209059.1, RCV000209447.1,