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rs67414444

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs67414444(A;A)
Make rs67414444(A;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38411938
GeneOTC
is asnp
is mentioned by
dbSNPrs67414444
ebirs67414444
HLIrs67414444
Exacrs67414444
Varsomers67414444
Maprs67414444
PheGenIrs67414444
hapmaprs67414444
1000 genomesrs67414444
hgdprs67414444
ensemblrs67414444
gopubmedrs67414444
geneviewrs67414444
scholarrs67414444
googlers67414444
pharmgkbrs67414444
gwascentralrs67414444
openSNPrs67414444
23andMers67414444
23andMe allrs67414444
SNP Nexus

SNPshotrs67414444
SNPdbers67414444
MSV3drs67414444
GWAS Ctlgrs67414444
Max Magnitude0
ClinVar
Risk rs67414444(A,G;A,G)
Alt rs67414444(A,G;A,G)
Reference rs67414444(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38271191T>A; NC_000023.10:g.38271191T>G
CLNSRC ClinVar
CLNACC RCV000083615.1, RCV000083616.1,



[PMID 11793468] Mutations and polymorphisms in the human ornithine transcarbamylase gene.