Have questions? Visit https://www.reddit.com/r/SNPedia

rs72558491

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs72558491(A;A)
Make rs72558491(A;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38421045
GeneOTC
is asnp
is mentioned by
dbSNPrs72558491
ebirs72558491
HLIrs72558491
Exacrs72558491
Varsomers72558491
Maprs72558491
PheGenIrs72558491
hapmaprs72558491
1000 genomesrs72558491
hgdprs72558491
ensemblrs72558491
gopubmedrs72558491
geneviewrs72558491
scholarrs72558491
googlers72558491
pharmgkbrs72558491
gwascentralrs72558491
openSNPrs72558491
23andMers72558491
23andMe allrs72558491
SNP Nexus

SNPshotrs72558491
SNPdbers72558491
MSV3drs72558491
GWAS Ctlgrs72558491
Max Magnitude0
ClinVar
Risk rs72558491(A;A)
Alt rs72558491(A;A)
Reference rs72558491(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38280298C>A
CLNSRC ClinVar
CLNACC RCV000083323.1,