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rs797044776

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044776(C;T)
Make rs797044776(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101398012
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs797044776
ebirs797044776
HLIrs797044776
Exacrs797044776
Varsomers797044776
Maprs797044776
PheGenIrs797044776
hapmaprs797044776
1000 genomesrs797044776
hgdprs797044776
ensemblrs797044776
gopubmedrs797044776
geneviewrs797044776
scholarrs797044776
googlers797044776
pharmgkbrs797044776
gwascentralrs797044776
openSNPrs797044776
23andMers797044776
23andMe allrs797044776
SNP Nexus

SNPshotrs797044776
SNPdbers797044776
MSV3drs797044776
GWAS Ctlgrs797044776
Max Magnitude0
ClinVar
Risk rs797044776(T;T)
Alt rs797044776(T;T)
Reference rs797044776(C;C)
Significance Pathogenic
Disease Fabry disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry disease
Reversed 1
HGVS NC_000023.10:g.100653000G>A
CLNSRC
CLNACC RCV000179729.1,