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

rs398123198

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs398123198(-;-)
Make rs398123198(-;TC)
ReferenceGRCh38 38.1/141
ChromosomeX
Position101398065
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs398123198
ebirs398123198
HLIrs398123198
Exacrs398123198
Varsomers398123198
Maprs398123198
PheGenIrs398123198
hapmaprs398123198
1000 genomesrs398123198
hgdprs398123198
ensemblrs398123198
gopubmedrs398123198
geneviewrs398123198
scholarrs398123198
googlers398123198
pharmgkbrs398123198
gwascentralrs398123198
openSNPrs398123198
23andMers398123198
23andMe allrs398123198
SNP Nexus

SNPshotrs398123198
SNPdbers398123198
MSV3drs398123198
GWAS Ctlgrs398123198
Max Magnitude0
ClinVar
Risk rs398123198(;)
Alt rs398123198(;)
Reference rs398123198(TC;TC)
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.100653053_100653054delGA
CLNSRC HGMD
CLNACC RCV000078263.6, RCV000236755.1,