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

rs797044774

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044774(A;A)
Make rs797044774(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101398027
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs797044774
ebirs797044774
HLIrs797044774
Exacrs797044774
Varsomers797044774
Maprs797044774
PheGenIrs797044774
hapmaprs797044774
1000 genomesrs797044774
hgdprs797044774
ensemblrs797044774
gopubmedrs797044774
geneviewrs797044774
scholarrs797044774
googlers797044774
pharmgkbrs797044774
gwascentralrs797044774
openSNPrs797044774
23andMers797044774
23andMe allrs797044774
SNP Nexus

SNPshotrs797044774
SNPdbers797044774
MSV3drs797044774
GWAS Ctlgrs797044774
Max Magnitude0
ClinVar
Risk rs797044774(A;A)
Alt rs797044774(A;A)
Reference rs797044774(G;G)
Significance Pathogenic
Disease Fabry disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry disease
Reversed 1
HGVS NC_000023.10:g.100653015C>T
CLNSRC University of Rostock
CLNACC RCV000179727.3,