Have questions? Visit https://www.reddit.com/r/SNPedia

rs120074112

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs120074112(A;G)
Make rs120074112(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position44948479
GeneAPOC2, INPP4B
is asnp
is mentioned by
dbSNPrs120074112
ebirs120074112
HLIrs120074112
Exacrs120074112
Varsomers120074112
Maprs120074112
PheGenIrs120074112
hapmaprs120074112
1000 genomesrs120074112
hgdprs120074112
ensemblrs120074112
gopubmedrs120074112
geneviewrs120074112
scholarrs120074112
googlers120074112
pharmgkbrs120074112
gwascentralrs120074112
openSNPrs120074112
23andMers120074112
23andMe allrs120074112
SNP Nexus

SNPshotrs120074112
SNPdbers120074112
MSV3drs120074112
GWAS Ctlgrs120074112
Max Magnitude0
OMIM608083
Desc
Variant0007
Relatedalso
ClinVar
Risk rs120074112(G;G)
Alt rs120074112(G;G)
Reference rs120074112(A;A)
Significance Pathogenic
Disease APOLIPOPROTEIN C-II (PARIS) Apolipoprotein C2 deficiency
Variation info
Gene APOC2 APOC4-APOC2
CLNDBN APOLIPOPROTEIN C-II (PARIS) Apolipoprotein C2 deficiency
Reversed 0
HGVS NC_000019.9:g.45451736A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000002693.2, RCV000002694.2,