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rs72558494

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72558494(C;T)
Make rs72558494(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38421059
GeneOTC
is asnp
is mentioned by
dbSNPrs72558494
ebirs72558494
HLIrs72558494
Exacrs72558494
Varsomers72558494
Maprs72558494
PheGenIrs72558494
hapmaprs72558494
1000 genomesrs72558494
hgdprs72558494
ensemblrs72558494
gopubmedrs72558494
geneviewrs72558494
scholarrs72558494
googlers72558494
pharmgkbrs72558494
gwascentralrs72558494
openSNPrs72558494
23andMers72558494
23andMe allrs72558494
SNP Nexus

SNPshotrs72558494
SNPdbers72558494
MSV3drs72558494
GWAS Ctlgrs72558494
Max Magnitude0
ClinVar
Risk rs72558494(T;T)
Alt rs72558494(T;T)
Reference rs72558494(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38280312C>T
CLNSRC ClinVar
CLNACC RCV000083328.1,