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

rs398123220

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123220(A;A)
Make rs398123220(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position101398852
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs398123220
ClinGenrs398123220
ebirs398123220
HLIrs398123220
Exacrs398123220
Varsomers398123220
Maprs398123220
PheGenIrs398123220
hapmaprs398123220
1000 genomesrs398123220
hgdprs398123220
ensemblrs398123220
gopubmedrs398123220
geneviewrs398123220
scholarrs398123220
googlers398123220
pharmgkbrs398123220
gwascentralrs398123220
openSNPrs398123220
23andMers398123220
23andMe allrs398123220
SNP Nexus

SNPshotrs398123220
SNPdbers398123220
MSV3drs398123220
GWAS Ctlgrs398123220
Max Magnitude0
ClinVar
Risk rs398123220(A;A) rs398123220(T;T)
Alt rs398123220(A;A) rs398123220(T;T)
Reference Rs398123220(G;G)
Significance Pathogenic
Disease not provided Fabry disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN not provided Fabry disease
Reversed 1
HGVS NC_000023.10:g.100653840C>A; NC_000023.10:g.100653840C>T
CLNSRC HGMD
CLNACC RCV000078296.4, RCV000078295.4,