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rs869312149

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869312149(A;G)
Make rs869312149(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101400667
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs869312149
ebirs869312149
HLIrs869312149
Exacrs869312149
Varsomers869312149
Maprs869312149
PheGenIrs869312149
hapmaprs869312149
1000 genomesrs869312149
hgdprs869312149
ensemblrs869312149
gopubmedrs869312149
geneviewrs869312149
scholarrs869312149
googlers869312149
pharmgkbrs869312149
gwascentralrs869312149
openSNPrs869312149
23andMers869312149
23andMe allrs869312149
SNP Nexus

SNPshotrs869312149
SNPdbers869312149
MSV3drs869312149
GWAS Ctlgrs869312149
Max Magnitude0
ClinVar
Risk rs869312149(G,T;G,T)
Alt rs869312149(G,T;G,T)
Reference rs869312149(A;A)
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.100655655T>C
CLNSRC
CLNACC RCV000209142.1, RCV000209822.1,