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rs797044702

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044702(C;T)
Make rs797044702(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101401710
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs797044702
ebirs797044702
HLIrs797044702
Exacrs797044702
Varsomers797044702
Maprs797044702
PheGenIrs797044702
hapmaprs797044702
1000 genomesrs797044702
hgdprs797044702
ensemblrs797044702
gopubmedrs797044702
geneviewrs797044702
scholarrs797044702
googlers797044702
pharmgkbrs797044702
gwascentralrs797044702
openSNPrs797044702
23andMers797044702
23andMe allrs797044702
SNP Nexus

SNPshotrs797044702
SNPdbers797044702
MSV3drs797044702
GWAS Ctlgrs797044702
Max Magnitude0
ClinVar
Risk rs797044702(T;T)
Alt rs797044702(T;T)
Reference rs797044702(C;C)
Significance Pathogenic
Disease Fabry disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry disease
Reversed 1
HGVS NC_000023.10:g.100656698G>A
CLNSRC
CLNACC RCV000176998.1,