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rs72556261

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs72556261(A;A)
Make rs72556261(A;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38401313
GeneOTC
is asnp
is mentioned by
dbSNPrs72556261
ebirs72556261
HLIrs72556261
Exacrs72556261
Varsomers72556261
Maprs72556261
PheGenIrs72556261
hapmaprs72556261
1000 genomesrs72556261
hgdprs72556261
ensemblrs72556261
gopubmedrs72556261
geneviewrs72556261
scholarrs72556261
googlers72556261
pharmgkbrs72556261
gwascentralrs72556261
openSNPrs72556261
23andMers72556261
23andMe allrs72556261
SNP Nexus

SNPshotrs72556261
SNPdbers72556261
MSV3drs72556261
GWAS Ctlgrs72556261
Max Magnitude0
ClinVar
Risk rs72556261(A,G;A,G)
Alt rs72556261(A,G;A,G)
Reference rs72556261(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38260566T>A
CLNSRC ClinVar
CLNACC RCV000083436.1,