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rs797044497

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797044497(A;C)
Make rs797044497(C;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101398076
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs797044497
ebirs797044497
HLIrs797044497
Exacrs797044497
Varsomers797044497
Maprs797044497
PheGenIrs797044497
hapmaprs797044497
1000 genomesrs797044497
hgdprs797044497
ensemblrs797044497
gopubmedrs797044497
geneviewrs797044497
scholarrs797044497
googlers797044497
pharmgkbrs797044497
gwascentralrs797044497
openSNPrs797044497
23andMers797044497
23andMe allrs797044497
SNP Nexus

SNPshotrs797044497
SNPdbers797044497
MSV3drs797044497
GWAS Ctlgrs797044497
Max Magnitude0
ClinVar
Risk rs797044497(C;C)
Alt rs797044497(C;C)
Reference rs797044497(A;A)
Significance Pathogenic
Disease Fabry disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry disease
Reversed 1
HGVS NC_000023.10:g.100653064T>G
CLNSRC HGMD
CLNACC RCV000153316.3,