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rs72558441

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72558441(C;C)
Make rs72558441(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38408937
GeneOTC
is asnp
is mentioned by
dbSNPrs72558441
ebirs72558441
HLIrs72558441
Exacrs72558441
Varsomers72558441
Maprs72558441
PheGenIrs72558441
hapmaprs72558441
1000 genomesrs72558441
hgdprs72558441
ensemblrs72558441
gopubmedrs72558441
geneviewrs72558441
scholarrs72558441
googlers72558441
pharmgkbrs72558441
gwascentralrs72558441
openSNPrs72558441
23andMers72558441
23andMe allrs72558441
SNP Nexus

SNPshotrs72558441
SNPdbers72558441
MSV3drs72558441
GWAS Ctlgrs72558441
Max Magnitude0
ClinVar
Risk rs72558441(C;C)
Alt rs72558441(C;C)
Reference rs72558441(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38268190T>C
CLNSRC ClinVar
CLNACC RCV000083564.1,