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rs72558432

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72558432(A;G)
Make rs72558432(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38408798
GeneOTC
is asnp
is mentioned by
dbSNPrs72558432
ebirs72558432
HLIrs72558432
Exacrs72558432
Varsomers72558432
Maprs72558432
PheGenIrs72558432
hapmaprs72558432
1000 genomesrs72558432
hgdprs72558432
ensemblrs72558432
gopubmedrs72558432
geneviewrs72558432
scholarrs72558432
googlers72558432
pharmgkbrs72558432
gwascentralrs72558432
openSNPrs72558432
23andMers72558432
23andMe allrs72558432
SNP Nexus

SNPshotrs72558432
SNPdbers72558432
MSV3drs72558432
GWAS Ctlgrs72558432
Max Magnitude0
ClinVar
Risk rs72558432(G;G)
Alt rs72558432(G;G)
Reference rs72558432(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38268051A>G
CLNSRC ClinVar
CLNACC RCV000083545.1,