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rs869312135

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869312135(C;C)
Make rs869312135(C;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101407842
GeneGLA, HNRNPH2, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs869312135
ebirs869312135
HLIrs869312135
Exacrs869312135
Varsomers869312135
Maprs869312135
PheGenIrs869312135
hapmaprs869312135
1000 genomesrs869312135
hgdprs869312135
ensemblrs869312135
gopubmedrs869312135
geneviewrs869312135
scholarrs869312135
googlers869312135
pharmgkbrs869312135
gwascentralrs869312135
openSNPrs869312135
23andMers869312135
23andMe allrs869312135
SNP Nexus

SNPshotrs869312135
SNPdbers869312135
MSV3drs869312135
GWAS Ctlgrs869312135
Max Magnitude0
ClinVar
Risk rs869312135(C;C)
Alt rs869312135(C;C)
Reference rs869312135(T;T)
Significance Drug-response
Disease Fabry disease Deoxygalactonojirimycin response
Variation info
Gene HNRNPH2 RPL36A-HNRNPH2 GLA
CLNDBN Fabry disease Deoxygalactonojirimycin response
Reversed 1
HGVS NC_000023.10:g.100662830A>G
CLNSRC
CLNACC RCV000209283.1, RCV000209546.1,