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rs72556276

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72556276(A;A)
Make rs72556276(A;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401392
GeneOTC
is asnp
is mentioned by
dbSNPrs72556276
ebirs72556276
HLIrs72556276
Exacrs72556276
Varsomers72556276
Maprs72556276
PheGenIrs72556276
hapmaprs72556276
1000 genomesrs72556276
hgdprs72556276
ensemblrs72556276
gopubmedrs72556276
geneviewrs72556276
scholarrs72556276
googlers72556276
pharmgkbrs72556276
gwascentralrs72556276
openSNPrs72556276
23andMers72556276
23andMe allrs72556276
SNP Nexus

SNPshotrs72556276
SNPdbers72556276
MSV3drs72556276
GWAS Ctlgrs72556276
Max Magnitude0
ClinVar
Risk rs72556276(A;A)
Alt rs72556276(A;A)
Reference rs72556276(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260645T>A
CLNSRC ClinVar
CLNACC RCV000083466.1,