rs878853973

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;G)	3	Carrier of a hypobetalipoproteinemia mutation
(G;G)	0	common in clinvar

Make rs878853973(-;-)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

21007345

Gene

APOB

is a	snp
is	mentioned by
dbSNP	rs878853973
dbSNP (classic)	rs878853973
ClinGen	rs878853973
ebi	rs878853973
HLI	rs878853973
Exac	rs878853973
Gnomad	rs878853973
Varsome	rs878853973
LitVar	rs878853973
Map	rs878853973
PheGenI	rs878853973
Biobank	rs878853973
1000 genomes	rs878853973
hgdp	rs878853973
ensembl	rs878853973
geneview	rs878853973
scholar	rs878853973
google	rs878853973
pharmgkb	rs878853973
gwascentral	rs878853973
openSNP	rs878853973
23andMe	rs878853973
SNPshot	rs878853973
SNPdbe	rs878853973
MSV3d	rs878853973
GWAS Ctlg	rs878853973

Max Magnitude

3

ClinVar
Risk	rs878853973(-;-)
Alt	rs878853973(-;-)
Reference	Rs878853973(G;G)
Significance	Pathogenic
Disease	Hypobetalipoproteinemia
Variation	info
Gene	APOB
CLNDBN	Hypobetalipoproteinemia, familial, 1
Reversed	1
HGVS	NC_000002.11:g.21230217delC
CLNSRC
CLNACC	RCV000227662.2,