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rs782449839

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs782449839(C;G)
Make rs782449839(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101397903
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs782449839
ebirs782449839
HLIrs782449839
Exacrs782449839
Varsomers782449839
Maprs782449839
PheGenIrs782449839
hapmaprs782449839
1000 genomesrs782449839
hgdprs782449839
ensemblrs782449839
gopubmedrs782449839
geneviewrs782449839
scholarrs782449839
googlers782449839
pharmgkbrs782449839
gwascentralrs782449839
openSNPrs782449839
23andMers782449839
23andMe allrs782449839
SNP Nexus

SNPshotrs782449839
SNPdbers782449839
MSV3drs782449839
GWAS Ctlgrs782449839
Max Magnitude0
ClinVar
Risk rs782449839(G;G)
Alt rs782449839(G;G)
Reference rs782449839(C;C)
Significance Drug-response
Disease Deoxygalactonojirimycin response Fabry disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Deoxygalactonojirimycin response Fabry disease
Reversed 0
HGVS NC_000023.10:g.100652891C>G
CLNSRC
CLNACC RCV000208881.1, RCV000209559.1,