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rs67294956

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs67294956(-;-)
Make rs67294956(-;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403660
GeneOTC
is asnp
is mentioned by
dbSNPrs67294956
ebirs67294956
HLIrs67294956
Exacrs67294956
Varsomers67294956
Maprs67294956
PheGenIrs67294956
hapmaprs67294956
1000 genomesrs67294956
hgdprs67294956
ensemblrs67294956
gopubmedrs67294956
geneviewrs67294956
scholarrs67294956
googlers67294956
pharmgkbrs67294956
gwascentralrs67294956
openSNPrs67294956
23andMers67294956
23andMe allrs67294956
SNP Nexus

SNPshotrs67294956
SNPdbers67294956
MSV3drs67294956
GWAS Ctlgrs67294956
Max Magnitude0
ClinVar
Risk rs67294956(;)
Alt rs67294956(;)
Reference rs67294956(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262913delG
CLNSRC ClinVar
CLNACC RCV000083498.1,