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rs869312145

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312145(G;T)
Make rs869312145(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101401639
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs869312145
ebirs869312145
HLIrs869312145
Exacrs869312145
Varsomers869312145
Maprs869312145
PheGenIrs869312145
hapmaprs869312145
1000 genomesrs869312145
hgdprs869312145
ensemblrs869312145
gopubmedrs869312145
geneviewrs869312145
scholarrs869312145
googlers869312145
pharmgkbrs869312145
gwascentralrs869312145
openSNPrs869312145
23andMers869312145
23andMe allrs869312145
SNP Nexus

SNPshotrs869312145
SNPdbers869312145
MSV3drs869312145
GWAS Ctlgrs869312145
Max Magnitude0
ClinVar
Risk rs869312145(T;T)
Alt rs869312145(T;T)
Reference rs869312145(G;G)
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.100656627C>A
CLNSRC
CLNACC RCV000209274.1, RCV000209663.1,