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rs72556287

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72556287(C;C)
Make rs72556287(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401428
GeneOTC
is asnp
is mentioned by
dbSNPrs72556287
ebirs72556287
HLIrs72556287
Exacrs72556287
Varsomers72556287
Maprs72556287
PheGenIrs72556287
hapmaprs72556287
1000 genomesrs72556287
hgdprs72556287
ensemblrs72556287
gopubmedrs72556287
geneviewrs72556287
scholarrs72556287
googlers72556287
pharmgkbrs72556287
gwascentralrs72556287
openSNPrs72556287
23andMers72556287
23andMe allrs72556287
SNP Nexus

SNPshotrs72556287
SNPdbers72556287
MSV3drs72556287
GWAS Ctlgrs72556287
Max Magnitude0
ClinVar
Risk rs72556287(C;C)
Alt rs72556287(C;C)
Reference rs72556287(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260681G>C
CLNSRC ClinVar
CLNACC RCV000083483.1,