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rs111060774

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GCTCTTTACATGTAAA;GCTCTTTACATGTAAA) 0 common in clinvar
(TCTTTACATGTAAAGC;TCTTTACATGTAAAGC) 0 common in clinvar
Make rs111060774(-;-)
Make rs111060774(-;TCTTTACATGTAAAGC)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38408802
GeneOTC
is asnp
is mentioned by
dbSNPrs111060774
ebirs111060774
HLIrs111060774
Exacrs111060774
Varsomers111060774
Maprs111060774
PheGenIrs111060774
hapmaprs111060774
1000 genomesrs111060774
hgdprs111060774
ensemblrs111060774
gopubmedrs111060774
geneviewrs111060774
scholarrs111060774
googlers111060774
pharmgkbrs111060774
gwascentralrs111060774
openSNPrs111060774
23andMers111060774
23andMe allrs111060774
SNP Nexus

SNPshotrs111060774
SNPdbers111060774
MSV3drs111060774
GWAS Ctlgrs111060774
Max Magnitude0
ClinVar
Risk rs111060774(;)
Alt rs111060774(;)
Reference rs111060774(GCTCTTTACATGTAAA;GCTCTTTACATGTAAA)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38268055_38268070del16
CLNSRC ClinVar
CLNACC RCV000083546.1,