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rs67870245

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs67870245(-;-)
Make rs67870245(-;C)
ReferenceGRCh38 38.1/141
ChromosomeX
Position38411900
GeneOTC
is asnp
is mentioned by
dbSNPrs67870245
ebirs67870245
HLIrs67870245
Exacrs67870245
Varsomers67870245
Maprs67870245
PheGenIrs67870245
hapmaprs67870245
1000 genomesrs67870245
hgdprs67870245
ensemblrs67870245
gopubmedrs67870245
geneviewrs67870245
scholarrs67870245
googlers67870245
pharmgkbrs67870245
gwascentralrs67870245
openSNPrs67870245
23andMers67870245
23andMe allrs67870245
SNP Nexus

SNPshotrs67870245
SNPdbers67870245
MSV3drs67870245
GWAS Ctlgrs67870245
Max Magnitude0
ClinVar
Risk rs67870245(;)
Alt rs67870245(;)
Reference rs67870245(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38271153delC
CLNSRC ClinVar
CLNACC RCV000083603.1,