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rs398123210

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398123210(A;G)
Make rs398123210(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position101401670
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs398123210
ebirs398123210
HLIrs398123210
Exacrs398123210
Varsomers398123210
Maprs398123210
PheGenIrs398123210
hapmaprs398123210
1000 genomesrs398123210
hgdprs398123210
ensemblrs398123210
gopubmedrs398123210
geneviewrs398123210
scholarrs398123210
googlers398123210
pharmgkbrs398123210
gwascentralrs398123210
openSNPrs398123210
23andMers398123210
23andMe allrs398123210
SNP Nexus

SNPshotrs398123210
SNPdbers398123210
MSV3drs398123210
GWAS Ctlgrs398123210
Max Magnitude0
ClinVar
Risk rs398123210(G;G)
Alt rs398123210(G;G)
Reference rs398123210(A;A)
Significance Pathogenic
Disease Fabry disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry disease
Reversed 1
HGVS NC_000023.10:g.100656658T>C
CLNSRC ClinVar Emory University
CLNACC RCV000078281.4,