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rs796052012

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052012(C;C)
Make rs796052012(C;G)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position38403692
GeneOTC
is asnp
is mentioned by
dbSNPrs796052012
ebirs796052012
HLIrs796052012
Exacrs796052012
Varsomers796052012
Maprs796052012
PheGenIrs796052012
hapmaprs796052012
1000 genomesrs796052012
hgdprs796052012
ensemblrs796052012
gopubmedrs796052012
geneviewrs796052012
scholarrs796052012
googlers796052012
pharmgkbrs796052012
gwascentralrs796052012
openSNPrs796052012
23andMers796052012
23andMe allrs796052012
SNP Nexus

SNPshotrs796052012
SNPdbers796052012
MSV3drs796052012
GWAS Ctlgrs796052012
Max Magnitude0
ClinVar
Risk rs796052012(C;C)
Alt rs796052012(C;C)
Reference rs796052012(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262945G>C
CLNSRC
CLNACC RCV000186067.2,