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rs869312154

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs869312154(C;C)
Make rs869312154(C;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101398802
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs869312154
ebirs869312154
HLIrs869312154
Exacrs869312154
Varsomers869312154
Maprs869312154
PheGenIrs869312154
hapmaprs869312154
1000 genomesrs869312154
hgdprs869312154
ensemblrs869312154
gopubmedrs869312154
geneviewrs869312154
scholarrs869312154
googlers869312154
pharmgkbrs869312154
gwascentralrs869312154
openSNPrs869312154
23andMers869312154
23andMe allrs869312154
SNP Nexus

SNPshotrs869312154
SNPdbers869312154
MSV3drs869312154
GWAS Ctlgrs869312154
Max Magnitude0
ClinVar
Risk rs869312154(C;C)
Alt rs869312154(C;C)
Reference rs869312154(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.100653790A>G
CLNSRC
CLNACC RCV000209382.1, RCV000209767.1,