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rs72554341

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72554341(A;A)
Make rs72554341(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38369848
GeneOTC
is asnp
is mentioned by
dbSNPrs72554341
ebirs72554341
HLIrs72554341
Exacrs72554341
Varsomers72554341
Maprs72554341
PheGenIrs72554341
hapmaprs72554341
1000 genomesrs72554341
hgdprs72554341
ensemblrs72554341
gopubmedrs72554341
geneviewrs72554341
scholarrs72554341
googlers72554341
pharmgkbrs72554341
gwascentralrs72554341
openSNPrs72554341
23andMers72554341
23andMe allrs72554341
SNP Nexus

SNPshotrs72554341
SNPdbers72554341
MSV3drs72554341
GWAS Ctlgrs72554341
Max Magnitude0
ClinVar
Risk rs72554341(A;A)
Alt rs72554341(A;A)
Reference rs72554341(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38229101G>A
CLNSRC ClinVar
CLNACC RCV000083379.1,