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rs397515873

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397515873(A;T)
Make rs397515873(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position101398862
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs397515873
ebirs397515873
HLIrs397515873
Exacrs397515873
Varsomers397515873
Maprs397515873
PheGenIrs397515873
hapmaprs397515873
1000 genomesrs397515873
hgdprs397515873
ensemblrs397515873
gopubmedrs397515873
geneviewrs397515873
scholarrs397515873
googlers397515873
pharmgkbrs397515873
gwascentralrs397515873
openSNPrs397515873
23andMers397515873
23andMe allrs397515873
SNP Nexus

SNPshotrs397515873
SNPdbers397515873
MSV3drs397515873
GWAS Ctlgrs397515873
Max Magnitude0
ClinVar
Risk rs397515873(T;T)
Alt rs397515873(T;T)
Reference rs397515873(A;A)
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.100653850T>A; NC_000023.10:g.100653850T>C
CLNSRC ClinVar
CLNACC RCV000035310.2, RCV000209315.1, RCV000209695.1,