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rs398123225

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(ATCA;ATCA) 0 common in clinvar
Make rs398123225(-;-)
Make rs398123225(-;ATCA)
ReferenceGRCh38 38.1/141
ChromosomeX
Position101398407
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs398123225
ClinGenrs398123225
ebirs398123225
HLIrs398123225
Exacrs398123225
Varsomers398123225
Maprs398123225
PheGenIrs398123225
hapmaprs398123225
1000 genomesrs398123225
hgdprs398123225
ensemblrs398123225
gopubmedrs398123225
geneviewrs398123225
scholarrs398123225
googlers398123225
pharmgkbrs398123225
gwascentralrs398123225
openSNPrs398123225
23andMers398123225
23andMe allrs398123225
SNP Nexus

SNPshotrs398123225
SNPdbers398123225
MSV3drs398123225
GWAS Ctlgrs398123225
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs398123225(ATCA;ATCA)
Significance Pathogenic
Disease Fabry disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry disease
Reversed 1
HGVS NC_000023.10:g.100653395_100653398delTGAT
CLNSRC ClinVar
CLNACC RCV000078303.4,