rs120074112

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs120074112(A;G)

Make rs120074112(G;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

44948479

Gene	APOC2, APOC4-APOC2

is a	snp
is	mentioned by
dbSNP	rs120074112
dbSNP (classic)	rs120074112
ClinGen	rs120074112
ebi	rs120074112
HLI	rs120074112
Exac	rs120074112
Gnomad	rs120074112
Varsome	rs120074112
LitVar	rs120074112
Map	rs120074112
PheGenI	rs120074112
Biobank	rs120074112
1000 genomes	rs120074112
hgdp	rs120074112
ensembl	rs120074112
geneview	rs120074112
scholar	rs120074112
google	rs120074112
pharmgkb	rs120074112
gwascentral	rs120074112
openSNP	rs120074112
23andMe	rs120074112
SNPshot	rs120074112
SNPdbe	rs120074112
MSV3d	rs120074112
GWAS Ctlg	rs120074112

Max Magnitude

0

OMIM	608083
Desc
Variant	0007
Related	also

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,