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rs72556275

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72556275(G;T)
Make rs72556275(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401381
GeneOTC
is asnp
is mentioned by
dbSNPrs72556275
ebirs72556275
HLIrs72556275
Exacrs72556275
Varsomers72556275
Maprs72556275
PheGenIrs72556275
hapmaprs72556275
1000 genomesrs72556275
hgdprs72556275
ensemblrs72556275
gopubmedrs72556275
geneviewrs72556275
scholarrs72556275
googlers72556275
pharmgkbrs72556275
gwascentralrs72556275
openSNPrs72556275
23andMers72556275
23andMe allrs72556275
SNP Nexus

SNPshotrs72556275
SNPdbers72556275
MSV3drs72556275
GWAS Ctlgrs72556275
Max Magnitude0
ClinVar
Risk rs72556275(T;T)
Alt rs72556275(T;T)
Reference rs72556275(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260634G>T
CLNSRC ClinVar
CLNACC RCV000083461.1,