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rs72556268

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72556268(A;A)
Make rs72556268(A;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401352
GeneOTC
is asnp
is mentioned by
dbSNPrs72556268
ebirs72556268
HLIrs72556268
Exacrs72556268
Varsomers72556268
Maprs72556268
PheGenIrs72556268
hapmaprs72556268
1000 genomesrs72556268
hgdprs72556268
ensemblrs72556268
gopubmedrs72556268
geneviewrs72556268
scholarrs72556268
googlers72556268
pharmgkbrs72556268
gwascentralrs72556268
openSNPrs72556268
23andMers72556268
23andMe allrs72556268
SNP Nexus

SNPshotrs72556268
SNPdbers72556268
MSV3drs72556268
GWAS Ctlgrs72556268
Max Magnitude0
ClinVar
Risk rs72556268(A;A)
Alt rs72556268(A;A)
Reference rs72556268(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260605C>A
CLNSRC ClinVar
CLNACC RCV000083449.1,