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rs72558449

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72558449(C;C)
Make rs72558449(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38408961
GeneOTC
is asnp
is mentioned by
dbSNPrs72558449
ebirs72558449
HLIrs72558449
Exacrs72558449
Varsomers72558449
Maprs72558449
PheGenIrs72558449
hapmaprs72558449
1000 genomesrs72558449
hgdprs72558449
ensemblrs72558449
gopubmedrs72558449
geneviewrs72558449
scholarrs72558449
googlers72558449
pharmgkbrs72558449
gwascentralrs72558449
openSNPrs72558449
23andMers72558449
23andMe allrs72558449
SNP Nexus

SNPshotrs72558449
SNPdbers72558449
MSV3drs72558449
GWAS Ctlgrs72558449
Max Magnitude0
ClinVar
Risk rs72558449(C;C)
Alt rs72558449(C;C)
Reference rs72558449(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38268214T>C
CLNSRC ClinVar
CLNACC RCV000083580.1,