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rs796052015

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796052015(-;A)
Make rs796052015(A;A)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position38369794
GeneOTC
is asnp
is mentioned by
dbSNPrs796052015
dbSNP (old)rs796052015
ClinGenrs796052015
ebirs796052015
HLIrs796052015
Exacrs796052015
Gnomadrs796052015
Varsomers796052015
Maprs796052015
PheGenIrs796052015
Biobankrs796052015
1000 genomesrs796052015
hgdprs796052015
ensemblrs796052015
gopubmedrs796052015
geneviewrs796052015
scholarrs796052015
googlers796052015
pharmgkbrs796052015
gwascentralrs796052015
openSNPrs796052015
23andMers796052015
23andMe allrs796052015
SNP Nexus

SNPshotrs796052015
SNPdbers796052015
MSV3drs796052015
GWAS Ctlgrs796052015
Max Magnitude0
ClinVar
Risk rs796052015(A;A)
Alt rs796052015(A;A)
Reference Rs796052015(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38229047dupA
CLNSRC
CLNACC RCV000186070.1,