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rs398123206

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123206(C;C)
Make rs398123206(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position101403986
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs398123206
ebirs398123206
HLIrs398123206
Exacrs398123206
Varsomers398123206
Maprs398123206
PheGenIrs398123206
hapmaprs398123206
1000 genomesrs398123206
hgdprs398123206
ensemblrs398123206
gopubmedrs398123206
geneviewrs398123206
scholarrs398123206
googlers398123206
pharmgkbrs398123206
gwascentralrs398123206
openSNPrs398123206
23andMers398123206
23andMe allrs398123206
SNP Nexus

SNPshotrs398123206
SNPdbers398123206
MSV3drs398123206
GWAS Ctlgrs398123206
Max Magnitude0
ClinVar
Risk rs398123206(C;C)
Alt rs398123206(C;C)
Reference rs398123206(G;G)
Significance Pathogenic
Disease Fabry disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry disease
Reversed 1
HGVS NC_000023.10:g.100658974C>G
CLNSRC ClinVar
CLNACC RCV000078271.4,