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rs72556293

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72556293(A;G)
Make rs72556293(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403625
GeneOTC
is asnp
is mentioned by
dbSNPrs72556293
ebirs72556293
HLIrs72556293
Exacrs72556293
Varsomers72556293
Maprs72556293
PheGenIrs72556293
hapmaprs72556293
1000 genomesrs72556293
hgdprs72556293
ensemblrs72556293
gopubmedrs72556293
geneviewrs72556293
scholarrs72556293
googlers72556293
pharmgkbrs72556293
gwascentralrs72556293
openSNPrs72556293
23andMers72556293
23andMe allrs72556293
SNP Nexus

SNPshotrs72556293
SNPdbers72556293
MSV3drs72556293
GWAS Ctlgrs72556293
Max Magnitude0
ClinVar
Risk rs72556293(G;G)
Alt rs72556293(G;G)
Reference rs72556293(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262878A>G
CLNSRC ClinVar
CLNACC RCV000083488.1,