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rs281865553

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281865553(A;A)
Make rs281865553(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38411999
GeneOTC
is asnp
is mentioned by
dbSNPrs281865553
ebirs281865553
HLIrs281865553
Exacrs281865553
Varsomers281865553
Maprs281865553
PheGenIrs281865553
hapmaprs281865553
1000 genomesrs281865553
hgdprs281865553
ensemblrs281865553
gopubmedrs281865553
geneviewrs281865553
scholarrs281865553
googlers281865553
pharmgkbrs281865553
gwascentralrs281865553
openSNPrs281865553
23andMers281865553
23andMe allrs281865553
SNP Nexus

SNPshotrs281865553
SNPdbers281865553
MSV3drs281865553
GWAS Ctlgrs281865553
Max Magnitude0
ClinVar
Risk rs281865553(A;A)
Alt rs281865553(A;A)
Reference rs281865553(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38271252G>A
CLNSRC ClinVar
CLNACC RCV000083315.1,