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rs72556299

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72556299(A;A)
Make rs72556299(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38403655
GeneOTC
is asnp
is mentioned by
dbSNPrs72556299
ebirs72556299
HLIrs72556299
Exacrs72556299
Varsomers72556299
Maprs72556299
PheGenIrs72556299
hapmaprs72556299
1000 genomesrs72556299
hgdprs72556299
ensemblrs72556299
gopubmedrs72556299
geneviewrs72556299
scholarrs72556299
googlers72556299
pharmgkbrs72556299
gwascentralrs72556299
openSNPrs72556299
23andMers72556299
23andMe allrs72556299
SNP Nexus

SNPshotrs72556299
SNPdbers72556299
MSV3drs72556299
GWAS Ctlgrs72556299
Max Magnitude0
ClinVar
Risk rs72556299(A;A)
Alt rs72556299(A;A)
Reference rs72556299(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262908G>A
CLNSRC ClinVar
CLNACC RCV000083496.1,