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rs72556283

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72556283(A;G)
Make rs72556283(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401415
GeneOTC
is asnp
is mentioned by
dbSNPrs72556283
ebirs72556283
HLIrs72556283
Exacrs72556283
Varsomers72556283
Maprs72556283
PheGenIrs72556283
hapmaprs72556283
1000 genomesrs72556283
hgdprs72556283
ensemblrs72556283
gopubmedrs72556283
geneviewrs72556283
scholarrs72556283
googlers72556283
pharmgkbrs72556283
gwascentralrs72556283
openSNPrs72556283
23andMers72556283
23andMe allrs72556283
SNP Nexus

SNPshotrs72556283
SNPdbers72556283
MSV3drs72556283
GWAS Ctlgrs72556283
Max Magnitude0
ClinVar
Risk rs72556283(G;G)
Alt rs72556283(G;G)
Reference rs72556283(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260668A>G
CLNSRC ClinVar
CLNACC RCV000083475.1,