Have questions? Visit https://www.reddit.com/r/SNPedia

rs67839039

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs67839039(-;-)
Make rs67839039(-;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38408741
GeneOTC
is asnp
is mentioned by
dbSNPrs67839039
ebirs67839039
HLIrs67839039
Exacrs67839039
Varsomers67839039
Maprs67839039
PheGenIrs67839039
hapmaprs67839039
1000 genomesrs67839039
hgdprs67839039
ensemblrs67839039
gopubmedrs67839039
geneviewrs67839039
scholarrs67839039
googlers67839039
pharmgkbrs67839039
gwascentralrs67839039
openSNPrs67839039
23andMers67839039
23andMe allrs67839039
SNP Nexus

SNPshotrs67839039
SNPdbers67839039
MSV3drs67839039
GWAS Ctlgrs67839039
Max Magnitude0
ClinVar
Risk rs67839039(;)
Alt rs67839039(;)
Reference rs67839039(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38267994delG
CLNSRC ClinVar
CLNACC RCV000083533.1,