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rs72554317

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs72554317(A;G)
Make rs72554317(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38367368
GeneOTC
is asnp
is mentioned by
dbSNPrs72554317
ebirs72554317
HLIrs72554317
Exacrs72554317
Varsomers72554317
Maprs72554317
PheGenIrs72554317
hapmaprs72554317
1000 genomesrs72554317
hgdprs72554317
ensemblrs72554317
gopubmedrs72554317
geneviewrs72554317
scholarrs72554317
googlers72554317
pharmgkbrs72554317
gwascentralrs72554317
openSNPrs72554317
23andMers72554317
23andMe allrs72554317
SNP Nexus

SNPshotrs72554317
SNPdbers72554317
MSV3drs72554317
GWAS Ctlgrs72554317
Max Magnitude0
ClinVar
Risk rs72554317(G;G)
Alt rs72554317(G;G)
Reference rs72554317(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38226621A>G
CLNSRC ClinVar
CLNACC RCV000083349.1,