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rs111060773

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AGGTA;AGGTA) 0 common in clinvar
(GTAAG;GTAAG) 0 common in clinvar
Make rs111060773(-;-)
Make rs111060773(-;GTAAG)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38369878
GeneOTC
is asnp
is mentioned by
dbSNPrs111060773
ebirs111060773
HLIrs111060773
Exacrs111060773
Varsomers111060773
Maprs111060773
PheGenIrs111060773
hapmaprs111060773
1000 genomesrs111060773
hgdprs111060773
ensemblrs111060773
gopubmedrs111060773
geneviewrs111060773
scholarrs111060773
googlers111060773
pharmgkbrs111060773
gwascentralrs111060773
openSNPrs111060773
23andMers111060773
23andMe allrs111060773
SNP Nexus

SNPshotrs111060773
SNPdbers111060773
MSV3drs111060773
GWAS Ctlgrs111060773
Max Magnitude0
ClinVar
Risk rs111060773(;)
Alt rs111060773(;)
Reference rs111060773(AGGTA;AGGTA)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38229131_38229135delGTAAG
CLNSRC ClinVar
CLNACC RCV000083394.1,