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rs72556301

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72556301(A;A)
Make rs72556301(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403666
GeneOTC
is asnp
is mentioned by
dbSNPrs72556301
ebirs72556301
HLIrs72556301
Exacrs72556301
Varsomers72556301
Maprs72556301
PheGenIrs72556301
hapmaprs72556301
1000 genomesrs72556301
hgdprs72556301
ensemblrs72556301
gopubmedrs72556301
geneviewrs72556301
scholarrs72556301
googlers72556301
pharmgkbrs72556301
gwascentralrs72556301
openSNPrs72556301
23andMers72556301
23andMe allrs72556301
SNP Nexus

SNPshotrs72556301
SNPdbers72556301
MSV3drs72556301
GWAS Ctlgrs72556301
Max Magnitude0
ClinVar
Risk rs72556301(A;A)
Alt rs72556301(A;A)
Reference rs72556301(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262919G>A
CLNSRC ClinVar
CLNACC RCV000083502.1,