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rs72556291

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72556291(A;T)
Make rs72556291(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403622
GeneOTC
is asnp
is mentioned by
dbSNPrs72556291
ebirs72556291
HLIrs72556291
Exacrs72556291
Varsomers72556291
Maprs72556291
PheGenIrs72556291
hapmaprs72556291
1000 genomesrs72556291
hgdprs72556291
ensemblrs72556291
gopubmedrs72556291
geneviewrs72556291
scholarrs72556291
googlers72556291
pharmgkbrs72556291
gwascentralrs72556291
openSNPrs72556291
23andMers72556291
23andMe allrs72556291
SNP Nexus

SNPshotrs72556291
SNPdbers72556291
MSV3drs72556291
GWAS Ctlgrs72556291
Max Magnitude0
ClinVar
Risk rs72556291(T;T)
Alt rs72556291(T;T)
Reference rs72556291(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262875A>T
CLNSRC ClinVar
CLNACC RCV000083486.1,