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rs797044777

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs797044777(-;-)
Make rs797044777(-;CT)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101397863
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs797044777
ClinGenrs797044777
ebirs797044777
HLIrs797044777
Exacrs797044777
Varsomers797044777
Maprs797044777
PheGenIrs797044777
hapmaprs797044777
1000 genomesrs797044777
hgdprs797044777
ensemblrs797044777
gopubmedrs797044777
geneviewrs797044777
scholarrs797044777
googlers797044777
pharmgkbrs797044777
gwascentralrs797044777
openSNPrs797044777
23andMers797044777
23andMe allrs797044777
SNP Nexus

SNPshotrs797044777
SNPdbers797044777
MSV3drs797044777
GWAS Ctlgrs797044777
Max Magnitude0
ClinVar
Risk rs797044777(-;-)
Alt rs797044777(-;-)
Reference Rs797044777(CT;CT)
Significance Pathogenic
Disease Fabry disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry disease
Reversed 1
HGVS NC_000023.10:g.100652851_100652852delAG
CLNSRC University of Rostock
CLNACC RCV000179730.3,