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rs797044775

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797044775(A;C)
Make rs797044775(C;C)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101397942
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs797044775
ebirs797044775
HLIrs797044775
Exacrs797044775
Varsomers797044775
Maprs797044775
PheGenIrs797044775
hapmaprs797044775
1000 genomesrs797044775
hgdprs797044775
ensemblrs797044775
gopubmedrs797044775
geneviewrs797044775
scholarrs797044775
googlers797044775
pharmgkbrs797044775
gwascentralrs797044775
openSNPrs797044775
23andMers797044775
23andMe allrs797044775
SNP Nexus

SNPshotrs797044775
SNPdbers797044775
MSV3drs797044775
GWAS Ctlgrs797044775
Max Magnitude0
ClinVar
Risk rs797044775(C;C)
Alt rs797044775(C;C)
Reference rs797044775(A;A)
Significance Pathogenic
Disease Fabry disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry disease
Reversed 1
HGVS NC_000023.10:g.100652930T>G
CLNSRC
CLNACC RCV000179728.1,