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rs869312148

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869312148(C;C)
Make rs869312148(C;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101400695
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs869312148
ebirs869312148
HLIrs869312148
Exacrs869312148
Varsomers869312148
Maprs869312148
PheGenIrs869312148
hapmaprs869312148
1000 genomesrs869312148
hgdprs869312148
ensemblrs869312148
gopubmedrs869312148
geneviewrs869312148
scholarrs869312148
googlers869312148
pharmgkbrs869312148
gwascentralrs869312148
openSNPrs869312148
23andMers869312148
23andMe allrs869312148
SNP Nexus

SNPshotrs869312148
SNPdbers869312148
MSV3drs869312148
GWAS Ctlgrs869312148
Max Magnitude0
ClinVar
Risk rs869312148(C;C)
Alt rs869312148(C;C)
Reference rs869312148(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.100655683A>G
CLNSRC
CLNACC RCV000209164.1, RCV000209436.1,