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rs72558480

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72558480(A;A)
Make rs72558480(A;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38411988
GeneOTC
is asnp
is mentioned by
dbSNPrs72558480
ebirs72558480
HLIrs72558480
Exacrs72558480
Varsomers72558480
Maprs72558480
PheGenIrs72558480
hapmaprs72558480
1000 genomesrs72558480
hgdprs72558480
ensemblrs72558480
gopubmedrs72558480
geneviewrs72558480
scholarrs72558480
googlers72558480
pharmgkbrs72558480
gwascentralrs72558480
openSNPrs72558480
23andMers72558480
23andMe allrs72558480
SNP Nexus

SNPshotrs72558480
SNPdbers72558480
MSV3drs72558480
GWAS Ctlgrs72558480
Max Magnitude0
ClinVar
Risk rs72558480(A;A)
Alt rs72558480(A;A)
Reference rs72558480(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38271241T>A
CLNSRC ClinVar
CLNACC RCV000083627.1,