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rs72552302

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72552302(A;A)
Make rs72552302(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38352778
GeneOTC
is asnp
is mentioned by
dbSNPrs72552302
ebirs72552302
HLIrs72552302
Exacrs72552302
Varsomers72552302
Maprs72552302
PheGenIrs72552302
hapmaprs72552302
1000 genomesrs72552302
hgdprs72552302
ensemblrs72552302
gopubmedrs72552302
geneviewrs72552302
scholarrs72552302
googlers72552302
pharmgkbrs72552302
gwascentralrs72552302
openSNPrs72552302
23andMers72552302
23andMe allrs72552302
SNP Nexus

SNPshotrs72552302
SNPdbers72552302
MSV3drs72552302
GWAS Ctlgrs72552302
Max Magnitude0
ClinVar
Risk rs72552302(A;A)
Alt rs72552302(A;A)
Reference rs72552302(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38212031G>A
CLNSRC ClinVar
CLNACC RCV000083563.1,