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rs72556272

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72556272(A;A)
Make rs72556272(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401373
GeneOTC
is asnp
is mentioned by
dbSNPrs72556272
ebirs72556272
HLIrs72556272
Exacrs72556272
Varsomers72556272
Maprs72556272
PheGenIrs72556272
hapmaprs72556272
1000 genomesrs72556272
hgdprs72556272
ensemblrs72556272
gopubmedrs72556272
geneviewrs72556272
scholarrs72556272
googlers72556272
pharmgkbrs72556272
gwascentralrs72556272
openSNPrs72556272
23andMers72556272
23andMe allrs72556272
SNP Nexus

SNPshotrs72556272
SNPdbers72556272
MSV3drs72556272
GWAS Ctlgrs72556272
Max Magnitude0
ClinVar
Risk rs72556272(A;A)
Alt rs72556272(A;A)
Reference rs72556272(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260626G>A
CLNSRC ClinVar
CLNACC RCV000083458.1,