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rs797044747

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044747(C;T)
Make rs797044747(T;T)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position101398925
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs797044747
ebirs797044747
HLIrs797044747
Exacrs797044747
Varsomers797044747
Maprs797044747
PheGenIrs797044747
hapmaprs797044747
1000 genomesrs797044747
hgdprs797044747
ensemblrs797044747
gopubmedrs797044747
geneviewrs797044747
scholarrs797044747
googlers797044747
pharmgkbrs797044747
gwascentralrs797044747
openSNPrs797044747
23andMers797044747
23andMe allrs797044747
SNP Nexus

SNPshotrs797044747
SNPdbers797044747
MSV3drs797044747
GWAS Ctlgrs797044747
Max Magnitude0
ClinVar
Risk rs797044747(T;T)
Alt rs797044747(T;T)
Reference rs797044747(C;C)
Significance Pathogenic
Disease Fabry disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry disease
Reversed 1
HGVS NC_000023.10:g.100653913G>A
CLNSRC
CLNACC RCV000178724.1,