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rs72556282

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72556282(C;C)
Make rs72556282(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401414
GeneOTC
is asnp
is mentioned by
dbSNPrs72556282
ebirs72556282
HLIrs72556282
Exacrs72556282
Varsomers72556282
Maprs72556282
PheGenIrs72556282
hapmaprs72556282
1000 genomesrs72556282
hgdprs72556282
ensemblrs72556282
gopubmedrs72556282
geneviewrs72556282
scholarrs72556282
googlers72556282
pharmgkbrs72556282
gwascentralrs72556282
openSNPrs72556282
23andMers72556282
23andMe allrs72556282
SNP Nexus

SNPshotrs72556282
SNPdbers72556282
MSV3drs72556282
GWAS Ctlgrs72556282
Max Magnitude0
ClinVar
Risk rs72556282(C;C)
Alt rs72556282(C;C)
Reference Rs72556282(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260667T>C
CLNSRC ClinVar
CLNACC RCV000083474.1,