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rs72556279

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72556279(A;T)
Make rs72556279(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401402
GeneOTC
is asnp
is mentioned by
dbSNPrs72556279
ebirs72556279
HLIrs72556279
Exacrs72556279
Varsomers72556279
Maprs72556279
PheGenIrs72556279
hapmaprs72556279
1000 genomesrs72556279
hgdprs72556279
ensemblrs72556279
gopubmedrs72556279
geneviewrs72556279
scholarrs72556279
googlers72556279
pharmgkbrs72556279
gwascentralrs72556279
openSNPrs72556279
23andMers72556279
23andMe allrs72556279
SNP Nexus

SNPshotrs72556279
SNPdbers72556279
MSV3drs72556279
GWAS Ctlgrs72556279
Max Magnitude0
ClinVar
Risk rs72556279(T;T)
Alt rs72556279(T;T)
Reference rs72556279(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260655A>T
CLNSRC ClinVar
CLNACC RCV000083469.1,