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rs281865552

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281865552(C;C)
Make rs281865552(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403740
GeneOTC
is asnp
is mentioned by
dbSNPrs281865552
ebirs281865552
HLIrs281865552
Exacrs281865552
Varsomers281865552
Maprs281865552
PheGenIrs281865552
hapmaprs281865552
1000 genomesrs281865552
hgdprs281865552
ensemblrs281865552
gopubmedrs281865552
geneviewrs281865552
scholarrs281865552
googlers281865552
pharmgkbrs281865552
gwascentralrs281865552
openSNPrs281865552
23andMers281865552
23andMe allrs281865552
SNP Nexus

SNPshotrs281865552
SNPdbers281865552
MSV3drs281865552
GWAS Ctlgrs281865552
Max Magnitude0
ClinVar
Risk rs281865552(A,C;A,C)
Alt rs281865552(A,C;A,C)
Reference rs281865552(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262993G>A; NC_000023.10:g.38262993G>C
CLNSRC ClinVar
CLNACC RCV000083530.1, RCV000083531.1,