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rs398123211

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs398123211(A;G)
Make rs398123211(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position101400759
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs398123211
ebirs398123211
HLIrs398123211
Exacrs398123211
Varsomers398123211
Maprs398123211
PheGenIrs398123211
hapmaprs398123211
1000 genomesrs398123211
hgdprs398123211
ensemblrs398123211
gopubmedrs398123211
geneviewrs398123211
scholarrs398123211
googlers398123211
pharmgkbrs398123211
gwascentralrs398123211
openSNPrs398123211
23andMers398123211
23andMe allrs398123211
SNP Nexus

SNPshotrs398123211
SNPdbers398123211
MSV3drs398123211
GWAS Ctlgrs398123211
Max Magnitude0
ClinVar
Risk rs398123211(G;G)
Alt rs398123211(G;G)
Reference rs398123211(A;A)
Significance Pathogenic
Disease Fabry disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry disease
Reversed 1
HGVS NC_000023.10:g.100655747T>C
CLNSRC HGMD
CLNACC RCV000078282.4,