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rs74518351

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs74518351(A;G)
Make rs74518351(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38367335
GeneOTC
is asnp
is mentioned by
dbSNPrs74518351
ebirs74518351
HLIrs74518351
Exacrs74518351
Varsomers74518351
Maprs74518351
PheGenIrs74518351
hapmaprs74518351
1000 genomesrs74518351
hgdprs74518351
ensemblrs74518351
gopubmedrs74518351
geneviewrs74518351
scholarrs74518351
googlers74518351
pharmgkbrs74518351
gwascentralrs74518351
openSNPrs74518351
23andMers74518351
23andMe allrs74518351
SNP Nexus

SNPshotrs74518351
SNPdbers74518351
MSV3drs74518351
GWAS Ctlgrs74518351
Max Magnitude0
ClinVar
Risk rs74518351(G;G)
Alt rs74518351(G;G)
Reference rs74518351(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38226588A>G
CLNSRC ClinVar
CLNACC RCV000083334.1,