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rs398123228

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123228(A;A)
Make rs398123228(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position101398395
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs398123228
ClinGenrs398123228
ebirs398123228
HLIrs398123228
Exacrs398123228
Varsomers398123228
Maprs398123228
PheGenIrs398123228
hapmaprs398123228
1000 genomesrs398123228
hgdprs398123228
ensemblrs398123228
gopubmedrs398123228
geneviewrs398123228
scholarrs398123228
googlers398123228
pharmgkbrs398123228
gwascentralrs398123228
openSNPrs398123228
23andMers398123228
23andMe allrs398123228
SNP Nexus

SNPshotrs398123228
SNPdbers398123228
MSV3drs398123228
GWAS Ctlgrs398123228
Max Magnitude0
ClinVar
Risk rs398123228(A;A)
Alt rs398123228(A;A)
Reference Rs398123228(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.100653383C>T
CLNSRC HGMD
CLNACC RCV000078306.4, RCV000157881.1,