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rs796052016

From SNPedia

Orientationplus
Make rs796052016(-;-)
Make rs796052016(-;GG)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position38403639
GeneOTC
is asnp
is mentioned by
dbSNPrs796052016
ebirs796052016
HLIrs796052016
Exacrs796052016
Varsomers796052016
Maprs796052016
PheGenIrs796052016
hapmaprs796052016
1000 genomesrs796052016
hgdprs796052016
ensemblrs796052016
gopubmedrs796052016
geneviewrs796052016
scholarrs796052016
googlers796052016
pharmgkbrs796052016
gwascentralrs796052016
openSNPrs796052016
23andMers796052016
23andMe allrs796052016
SNP Nexus

SNPshotrs796052016
SNPdbers796052016
MSV3drs796052016
GWAS Ctlgrs796052016
Max Magnitude
ClinVar
Risk rs796052016(;)
Alt rs796052016(;)
Reference rs796052016(GG;GG)
Significance Pathogenic
Disease not provided
Variation info
Gene OTC
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.38262892_38262893delGG
CLNSRC
CLNACC RCV000186071.1,