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rs72558403

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72558403(A;T)
Make rs72558403(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403670
GeneOTC
is asnp
is mentioned by
dbSNPrs72558403
ebirs72558403
HLIrs72558403
Exacrs72558403
Varsomers72558403
Maprs72558403
PheGenIrs72558403
hapmaprs72558403
1000 genomesrs72558403
hgdprs72558403
ensemblrs72558403
gopubmedrs72558403
geneviewrs72558403
scholarrs72558403
googlers72558403
pharmgkbrs72558403
gwascentralrs72558403
openSNPrs72558403
23andMers72558403
23andMe allrs72558403
SNP Nexus

SNPshotrs72558403
SNPdbers72558403
MSV3drs72558403
GWAS Ctlgrs72558403
Max Magnitude0
ClinVar
Risk rs72558403(T;T)
Alt rs72558403(T;T)
Reference rs72558403(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262923A>T
CLNSRC ClinVar
CLNACC RCV000083504.1,