Have questions? Visit https://www.reddit.com/r/SNPedia

rs727503072

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs727503072(C;C)
Make rs727503072(C;T)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position101401793
GeneGLA, RPL36A-HNRNPH2
is asnp
is mentioned by
dbSNPrs727503072
ebirs727503072
HLIrs727503072
Exacrs727503072
Varsomers727503072
Maprs727503072
PheGenIrs727503072
hapmaprs727503072
1000 genomesrs727503072
hgdprs727503072
ensemblrs727503072
gopubmedrs727503072
geneviewrs727503072
scholarrs727503072
googlers727503072
pharmgkbrs727503072
gwascentralrs727503072
openSNPrs727503072
23andMers727503072
23andMe allrs727503072
SNP Nexus

SNPshotrs727503072
SNPdbers727503072
MSV3drs727503072
GWAS Ctlgrs727503072
Max Magnitude0
ClinVar
Risk rs727503072(C;C)
Alt rs727503072(C;C)
Reference rs727503072(T;T)
Significance Probable-Pathogenic
Disease Fabry disease
Variation info
Gene RPL36A-HNRNPH2 GLA
CLNDBN Fabry disease
Reversed 1
HGVS NC_000023.10:g.100656781A>G
CLNSRC
CLNACC RCV000150748.1,