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

rs72556266

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72556266(C;T)
Make rs72556266(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401343
GeneOTC
is asnp
is mentioned by
dbSNPrs72556266
ebirs72556266
HLIrs72556266
Exacrs72556266
Varsomers72556266
Maprs72556266
PheGenIrs72556266
hapmaprs72556266
1000 genomesrs72556266
hgdprs72556266
ensemblrs72556266
gopubmedrs72556266
geneviewrs72556266
scholarrs72556266
googlers72556266
pharmgkbrs72556266
gwascentralrs72556266
openSNPrs72556266
23andMers72556266
23andMe allrs72556266
SNP Nexus

SNPshotrs72556266
SNPdbers72556266
MSV3drs72556266
GWAS Ctlgrs72556266
Max Magnitude0
ClinVar
Risk rs72556266(T;T)
Alt rs72556266(T;T)
Reference rs72556266(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260596C>T
CLNSRC ClinVar
CLNACC RCV000083445.1,