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rs781838005

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs781838005(C;T)
Make rs781838005(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101403941
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs781838005
ebirs781838005
HLIrs781838005
Exacrs781838005
Varsomers781838005
Maprs781838005
PheGenIrs781838005
hapmaprs781838005
1000 genomesrs781838005
hgdprs781838005
ensemblrs781838005
gopubmedrs781838005
geneviewrs781838005
scholarrs781838005
googlers781838005
pharmgkbrs781838005
gwascentralrs781838005
openSNPrs781838005
23andMers781838005
23andMe allrs781838005
SNP Nexus

SNPshotrs781838005
SNPdbers781838005
MSV3drs781838005
GWAS Ctlgrs781838005
Max Magnitude0
ClinVar
Risk rs781838005(T;T)
Alt rs781838005(T;T)
Reference rs781838005(C;C)
Significance Drug-response
Disease Fabry disease Deoxygalactonojirimycin response
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry disease Deoxygalactonojirimycin response
Reversed 0
HGVS NC_000023.10:g.100658929C>T
CLNSRC
CLNACC RCV000209421.1, RCV000209815.1,