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rs72556269

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72556269(C;C)
Make rs72556269(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401364
GeneOTC
is asnp
is mentioned by
dbSNPrs72556269
ebirs72556269
HLIrs72556269
Exacrs72556269
Varsomers72556269
Maprs72556269
PheGenIrs72556269
hapmaprs72556269
1000 genomesrs72556269
hgdprs72556269
ensemblrs72556269
gopubmedrs72556269
geneviewrs72556269
scholarrs72556269
googlers72556269
pharmgkbrs72556269
gwascentralrs72556269
openSNPrs72556269
23andMers72556269
23andMe allrs72556269
SNP Nexus

SNPshotrs72556269
SNPdbers72556269
MSV3drs72556269
GWAS Ctlgrs72556269
Max Magnitude0
ClinVar
Risk rs72556269(C;C)
Alt rs72556269(C;C)
Reference rs72556269(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260617T>C
CLNSRC ClinVar
CLNACC RCV000083450.1,