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rs72558453

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(I;I) 0
Make rs72558453(-;-)
Make rs72558453(-;A)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38408976
GeneOTC
is asnp
is mentioned by
dbSNPrs72558453
ebirs72558453
HLIrs72558453
Exacrs72558453
Varsomers72558453
Maprs72558453
PheGenIrs72558453
hapmaprs72558453
1000 genomesrs72558453
hgdprs72558453
ensemblrs72558453
gopubmedrs72558453
geneviewrs72558453
scholarrs72558453
googlers72558453
pharmgkbrs72558453
gwascentralrs72558453
openSNPrs72558453
23andMers72558453
23andMe allrs72558453
SNP Nexus

SNPshotrs72558453
SNPdbers72558453
MSV3drs72558453
GWAS Ctlgrs72558453
Max Magnitude0
ClinVar
Risk rs72558453(;)
Alt rs72558453(;)
Reference rs72558453(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38268229delA
CLNSRC ClinVar
CLNACC RCV000083585.1,