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rs869312137

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312137(A;A)
Make rs869312137(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101407800
GeneGLA, HNRNPH2, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs869312137
ebirs869312137
HLIrs869312137
Exacrs869312137
Varsomers869312137
Maprs869312137
PheGenIrs869312137
hapmaprs869312137
1000 genomesrs869312137
hgdprs869312137
ensemblrs869312137
gopubmedrs869312137
geneviewrs869312137
scholarrs869312137
googlers869312137
pharmgkbrs869312137
gwascentralrs869312137
openSNPrs869312137
23andMers869312137
23andMe allrs869312137
SNP Nexus

SNPshotrs869312137
SNPdbers869312137
MSV3drs869312137
GWAS Ctlgrs869312137
Max Magnitude0
ClinVar
Risk rs869312137(A;A)
Alt rs869312137(A;A)
Reference rs869312137(G;G)
Significance Drug-response
Disease Deoxygalactonojirimycin response Fabry disease
Variation info
Gene RPL36A-HNRNPH2 HNRNPH2 GLA
CLNDBN Deoxygalactonojirimycin response Fabry disease
Reversed 1
HGVS NC_000023.10:g.100662788C>T
CLNSRC
CLNACC RCV000208963.1, RCV000209648.1,