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

rs797044746

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044746(C;G)
Make rs797044746(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101398882
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs797044746
ebirs797044746
HLIrs797044746
Exacrs797044746
Varsomers797044746
Maprs797044746
PheGenIrs797044746
hapmaprs797044746
1000 genomesrs797044746
hgdprs797044746
ensemblrs797044746
gopubmedrs797044746
geneviewrs797044746
scholarrs797044746
googlers797044746
pharmgkbrs797044746
gwascentralrs797044746
openSNPrs797044746
23andMers797044746
23andMe allrs797044746
SNP Nexus

SNPshotrs797044746
SNPdbers797044746
MSV3drs797044746
GWAS Ctlgrs797044746
Max Magnitude0
ClinVar
Risk rs797044746(G;G)
Alt rs797044746(G;G)
Reference rs797044746(C;C)
Significance Probable-Pathogenic
Disease Fabry disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry disease
Reversed 1
HGVS NC_000023.10:g.100653870G>C
CLNSRC
CLNACC RCV000178723.1,