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rs796052013

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052013(A;G)
Make rs796052013(G;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position38411913
GeneOTC
is asnp
is mentioned by
dbSNPrs796052013
ebirs796052013
HLIrs796052013
Exacrs796052013
Varsomers796052013
Maprs796052013
PheGenIrs796052013
hapmaprs796052013
1000 genomesrs796052013
hgdprs796052013
ensemblrs796052013
gopubmedrs796052013
geneviewrs796052013
scholarrs796052013
googlers796052013
pharmgkbrs796052013
gwascentralrs796052013
openSNPrs796052013
23andMers796052013
23andMe allrs796052013
SNP Nexus

SNPshotrs796052013
SNPdbers796052013
MSV3drs796052013
GWAS Ctlgrs796052013
Max Magnitude0
ClinVar
Risk rs796052013(G;G)
Alt rs796052013(G;G)
Reference rs796052013(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38271166A>G
CLNSRC
CLNACC RCV000186068.2,