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rs398123212

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123212(G;T)
Make rs398123212(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position101400757
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs398123212
ebirs398123212
HLIrs398123212
Exacrs398123212
Varsomers398123212
Maprs398123212
PheGenIrs398123212
hapmaprs398123212
1000 genomesrs398123212
hgdprs398123212
ensemblrs398123212
gopubmedrs398123212
geneviewrs398123212
scholarrs398123212
googlers398123212
pharmgkbrs398123212
gwascentralrs398123212
openSNPrs398123212
23andMers398123212
23andMe allrs398123212
SNP Nexus

SNPshotrs398123212
SNPdbers398123212
MSV3drs398123212
GWAS Ctlgrs398123212
Max Magnitude0
ClinVar
Risk rs398123212(T;T)
Alt rs398123212(T;T)
Reference rs398123212(G;G)
Significance Pathogenic
Disease Fabry disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry disease
Reversed 1
HGVS NC_000023.10:g.100655745C>A
CLNSRC HGMD
CLNACC RCV000078283.4,