Have questions? Visit https://www.reddit.com/r/SNPedia

rs398123216

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123216(G;T)
Make rs398123216(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position101398947
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs398123216
ebirs398123216
HLIrs398123216
Exacrs398123216
Varsomers398123216
Maprs398123216
PheGenIrs398123216
hapmaprs398123216
1000 genomesrs398123216
hgdprs398123216
ensemblrs398123216
gopubmedrs398123216
geneviewrs398123216
scholarrs398123216
googlers398123216
pharmgkbrs398123216
gwascentralrs398123216
openSNPrs398123216
23andMers398123216
23andMe allrs398123216
SNP Nexus

SNPshotrs398123216
SNPdbers398123216
MSV3drs398123216
GWAS Ctlgrs398123216
Max Magnitude0
ClinVar
Risk rs398123216(T;T)
Alt rs398123216(T;T)
Reference rs398123216(G;G)
Significance Pathogenic
Disease Fabry disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry disease
Reversed 1
HGVS NC_000023.10:g.100653935C>A
CLNSRC HGMD
CLNACC RCV000078288.4,