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rs797044669

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797044669(A;A)
Make rs797044669(A;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101403810
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs797044669
ebirs797044669
HLIrs797044669
Exacrs797044669
Varsomers797044669
Maprs797044669
PheGenIrs797044669
hapmaprs797044669
1000 genomesrs797044669
hgdprs797044669
ensemblrs797044669
gopubmedrs797044669
geneviewrs797044669
scholarrs797044669
googlers797044669
pharmgkbrs797044669
gwascentralrs797044669
openSNPrs797044669
23andMers797044669
23andMe allrs797044669
SNP Nexus

SNPshotrs797044669
SNPdbers797044669
MSV3drs797044669
GWAS Ctlgrs797044669
Max Magnitude0
ClinVar
Risk rs797044669(A;A)
Alt rs797044669(A;A)
Reference rs797044669(G;G)
Significance Pathogenic
Disease Fabry disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry disease
Reversed 1
HGVS NC_000023.10:g.100658798C>T
CLNSRC University of Rostock
CLNACC RCV000175538.3,