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rs72556296

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72556296(C;T)
Make rs72556296(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403648
GeneOTC
is asnp
is mentioned by
dbSNPrs72556296
ebirs72556296
HLIrs72556296
Exacrs72556296
Varsomers72556296
Maprs72556296
PheGenIrs72556296
hapmaprs72556296
1000 genomesrs72556296
hgdprs72556296
ensemblrs72556296
gopubmedrs72556296
geneviewrs72556296
scholarrs72556296
googlers72556296
pharmgkbrs72556296
gwascentralrs72556296
openSNPrs72556296
23andMers72556296
23andMe allrs72556296
SNP Nexus

SNPshotrs72556296
SNPdbers72556296
MSV3drs72556296
GWAS Ctlgrs72556296
Max Magnitude0
ClinVar
Risk rs72556296(T;T)
Alt rs72556296(T;T)
Reference rs72556296(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262901C>T
CLNSRC ClinVar
CLNACC RCV000083491.1,