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rs72556302

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72556302(A;A)
Make rs72556302(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403667
GeneOTC
is asnp
is mentioned by
dbSNPrs72556302
ebirs72556302
HLIrs72556302
Exacrs72556302
Varsomers72556302
Maprs72556302
PheGenIrs72556302
hapmaprs72556302
1000 genomesrs72556302
hgdprs72556302
ensemblrs72556302
gopubmedrs72556302
geneviewrs72556302
scholarrs72556302
googlers72556302
pharmgkbrs72556302
gwascentralrs72556302
openSNPrs72556302
23andMers72556302
23andMe allrs72556302
SNP Nexus

SNPshotrs72556302
SNPdbers72556302
MSV3drs72556302
GWAS Ctlgrs72556302
Max Magnitude0
ClinVar
Risk rs72556302(A;A)
Alt rs72556302(A;A)
Reference rs72556302(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262920G>A
CLNSRC ClinVar
CLNACC RCV000083503.1,