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rs281865554

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs281865554(C;C)
Make rs281865554(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38367290
GeneOTC
is asnp
is mentioned by
dbSNPrs281865554
ebirs281865554
HLIrs281865554
Exacrs281865554
Varsomers281865554
Maprs281865554
PheGenIrs281865554
hapmaprs281865554
1000 genomesrs281865554
hgdprs281865554
ensemblrs281865554
gopubmedrs281865554
geneviewrs281865554
scholarrs281865554
googlers281865554
pharmgkbrs281865554
gwascentralrs281865554
openSNPrs281865554
23andMers281865554
23andMe allrs281865554
SNP Nexus

SNPshotrs281865554
SNPdbers281865554
MSV3drs281865554
GWAS Ctlgrs281865554
Max Magnitude0
ClinVar
Risk rs281865554(C;C)
Alt rs281865554(C;C)
Reference rs281865554(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38226543G>C
CLNSRC ClinVar
CLNACC RCV000083567.1,