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rs72556284

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72556284(C;T)
Make rs72556284(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401421
GeneOTC
is asnp
is mentioned by
dbSNPrs72556284
ebirs72556284
HLIrs72556284
Exacrs72556284
Varsomers72556284
Maprs72556284
PheGenIrs72556284
hapmaprs72556284
1000 genomesrs72556284
hgdprs72556284
ensemblrs72556284
gopubmedrs72556284
geneviewrs72556284
scholarrs72556284
googlers72556284
pharmgkbrs72556284
gwascentralrs72556284
openSNPrs72556284
23andMers72556284
23andMe allrs72556284
SNP Nexus

SNPshotrs72556284
SNPdbers72556284
MSV3drs72556284
GWAS Ctlgrs72556284
Max Magnitude0
ClinVar
Risk rs72556284(T;T)
Alt rs72556284(T;T)
Reference rs72556284(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260674C>T
CLNSRC ClinVar
CLNACC RCV000083477.1,