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rs72558418

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72558418(A;C)
Make rs72558418(C;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403705
GeneOTC
is asnp
is mentioned by
dbSNPrs72558418
ebirs72558418
HLIrs72558418
Exacrs72558418
Varsomers72558418
Maprs72558418
PheGenIrs72558418
hapmaprs72558418
1000 genomesrs72558418
hgdprs72558418
ensemblrs72558418
gopubmedrs72558418
geneviewrs72558418
scholarrs72558418
googlers72558418
pharmgkbrs72558418
gwascentralrs72558418
openSNPrs72558418
23andMers72558418
23andMe allrs72558418
SNP Nexus

SNPshotrs72558418
SNPdbers72558418
MSV3drs72558418
GWAS Ctlgrs72558418
Max Magnitude0
ClinVar
Risk rs72558418(C;C)
Alt rs72558418(C;C)
Reference rs72558418(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262958A>C
CLNSRC ClinVar
CLNACC RCV000083519.1,