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rs398123208

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123208(A;A)
Make rs398123208(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position101403938
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs398123208
ebirs398123208
HLIrs398123208
Exacrs398123208
Varsomers398123208
Maprs398123208
PheGenIrs398123208
hapmaprs398123208
1000 genomesrs398123208
hgdprs398123208
ensemblrs398123208
gopubmedrs398123208
geneviewrs398123208
scholarrs398123208
googlers398123208
pharmgkbrs398123208
gwascentralrs398123208
openSNPrs398123208
23andMers398123208
23andMe allrs398123208
SNP Nexus

SNPshotrs398123208
SNPdbers398123208
MSV3drs398123208
GWAS Ctlgrs398123208
Max Magnitude0
ClinVar
Risk rs398123208(A;A)
Alt rs398123208(A;A)
Reference rs398123208(G;G)
Significance Pathogenic
Disease Fabry disease not provided
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry disease not provided
Reversed 1
HGVS NC_000023.10:g.100658926C>T
CLNSRC HGMD
CLNACC RCV000078273.4, RCV000157886.2,