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rs120074114

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs120074114(A;C)
Make rs120074114(C;C)
ReferenceGRCh38 38.1/141
Chromosome19
Position44948767
GeneAPOC2, INPP4B
is asnp
is mentioned by
dbSNPrs120074114
ebirs120074114
HLIrs120074114
Exacrs120074114
Varsomers120074114
Maprs120074114
PheGenIrs120074114
hapmaprs120074114
1000 genomesrs120074114
hgdprs120074114
ensemblrs120074114
gopubmedrs120074114
geneviewrs120074114
scholarrs120074114
googlers120074114
pharmgkbrs120074114
gwascentralrs120074114
openSNPrs120074114
23andMers120074114
23andMe allrs120074114
SNP Nexus

SNPshotrs120074114
SNPdbers120074114
MSV3drs120074114
GWAS Ctlgrs120074114
GMAF0.0009183
Max Magnitude0
OMIM608083
Desc
Variant0009
Relatedalso
ClinVar
Risk rs120074114(C;C)
Alt rs120074114(C;C)
Reference rs120074114(A;A)
Significance Pathogenic
Disease Apolipoprotein c-ii variant
Variation info
Gene APOC2 APOC4-APOC2
CLNDBN Apolipoprotein c-ii variant
Reversed 0
HGVS NC_000019.9:g.45452024A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000002697.2,