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rs72556289

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72556289(A;G)
Make rs72556289(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403616
GeneOTC
is asnp
is mentioned by
dbSNPrs72556289
ebirs72556289
HLIrs72556289
Exacrs72556289
Varsomers72556289
Maprs72556289
PheGenIrs72556289
hapmaprs72556289
1000 genomesrs72556289
hgdprs72556289
ensemblrs72556289
gopubmedrs72556289
geneviewrs72556289
scholarrs72556289
googlers72556289
pharmgkbrs72556289
gwascentralrs72556289
openSNPrs72556289
23andMers72556289
23andMe allrs72556289
SNP Nexus

SNPshotrs72556289
SNPdbers72556289
MSV3drs72556289
GWAS Ctlgrs72556289
Max Magnitude0
ClinVar
Risk rs72556289(G;G)
Alt rs72556289(G;G)
Reference rs72556289(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262869A>G
CLNSRC ClinVar
CLNACC RCV000083484.1,