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rs869312153

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869312153(C;C)
Make rs869312153(C;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101398825
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs869312153
ebirs869312153
HLIrs869312153
Exacrs869312153
Varsomers869312153
Maprs869312153
PheGenIrs869312153
hapmaprs869312153
1000 genomesrs869312153
hgdprs869312153
ensemblrs869312153
gopubmedrs869312153
geneviewrs869312153
scholarrs869312153
googlers869312153
pharmgkbrs869312153
gwascentralrs869312153
openSNPrs869312153
23andMers869312153
23andMe allrs869312153
SNP Nexus

SNPshotrs869312153
SNPdbers869312153
MSV3drs869312153
GWAS Ctlgrs869312153
Max Magnitude0
ClinVar
Risk rs869312153(C;C)
Alt rs869312153(C;C)
Reference rs869312153(T;T)
Significance Drug-response
Disease Deoxygalactonojirimycin response Fabry disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Deoxygalactonojirimycin response Fabry disease
Reversed 1
HGVS NC_000023.10:g.100653813A>G
CLNSRC
CLNACC RCV000209113.1, RCV000209677.1,