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

rs72552298

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(I;I) 0
(T;T) 0 common in clinvar
Make rs72552298(-;-)
Make rs72552298(-;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38352736
GeneOTC
is asnp
is mentioned by
dbSNPrs72552298
ebirs72552298
HLIrs72552298
Exacrs72552298
Varsomers72552298
Maprs72552298
PheGenIrs72552298
hapmaprs72552298
1000 genomesrs72552298
hgdprs72552298
ensemblrs72552298
gopubmedrs72552298
geneviewrs72552298
scholarrs72552298
googlers72552298
pharmgkbrs72552298
gwascentralrs72552298
openSNPrs72552298
23andMers72552298
23andMe allrs72552298
SNP Nexus

SNPshotrs72552298
SNPdbers72552298
MSV3drs72552298
GWAS Ctlgrs72552298
Max Magnitude0
ClinVar
Risk rs72552298(;)
Alt rs72552298(;)
Reference rs72552298(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38211989delT
CLNSRC ClinVar
CLNACC RCV000083429.1,