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rs398123219

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123219(A;A)
Make rs398123219(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position101398909
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs398123219
ebirs398123219
HLIrs398123219
Exacrs398123219
Varsomers398123219
Maprs398123219
PheGenIrs398123219
hapmaprs398123219
1000 genomesrs398123219
hgdprs398123219
ensemblrs398123219
gopubmedrs398123219
geneviewrs398123219
scholarrs398123219
googlers398123219
pharmgkbrs398123219
gwascentralrs398123219
openSNPrs398123219
23andMers398123219
23andMe allrs398123219
SNP Nexus

SNPshotrs398123219
SNPdbers398123219
MSV3drs398123219
GWAS Ctlgrs398123219
Max Magnitude0
ClinVar
Risk rs398123219(A;A)
Alt rs398123219(A;A)
Reference rs398123219(G;G)
Significance Pathogenic
Disease Fabry disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry disease
Reversed 1
HGVS NC_000023.10:g.100653897C>T
CLNSRC HGMD
CLNACC RCV000078292.4,