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rs67294955

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs67294955(A;A)
Make rs67294955(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403660
GeneOTC
is asnp
is mentioned by
dbSNPrs67294955
ebirs67294955
HLIrs67294955
Exacrs67294955
Varsomers67294955
Maprs67294955
PheGenIrs67294955
hapmaprs67294955
1000 genomesrs67294955
hgdprs67294955
ensemblrs67294955
gopubmedrs67294955
geneviewrs67294955
scholarrs67294955
googlers67294955
pharmgkbrs67294955
gwascentralrs67294955
openSNPrs67294955
23andMers67294955
23andMe allrs67294955
SNP Nexus

SNPshotrs67294955
SNPdbers67294955
MSV3drs67294955
GWAS Ctlgrs67294955
Max Magnitude0
ClinVar
Risk rs67294955(A;A)
Alt rs67294955(A;A)
Reference rs67294955(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262913G>A
CLNSRC ClinVar
CLNACC RCV000083497.2,