rs2306986

Orientation

plus

Stabilized

plus

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

Make rs2306986(C;C)

Make rs2306986(C;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

99583418

Gene

MTTP

is a	snp
is	mentioned by
dbSNP	rs2306986
dbSNP (classic)	rs2306986
ClinGen	rs2306986
ebi	rs2306986
HLI	rs2306986
Exac	rs2306986
Gnomad	rs2306986
Varsome	rs2306986
LitVar	rs2306986
Map	rs2306986
PheGenI	rs2306986
Biobank	rs2306986
1000 genomes	rs2306986
hgdp	rs2306986
ensembl	rs2306986
geneview	rs2306986
scholar	rs2306986
google	rs2306986
pharmgkb	rs2306986
gwascentral	rs2306986
openSNP	rs2306986
23andMe	rs2306986
SNPshot	rs2306986
SNPdbe	rs2306986
MSV3d	rs2306986
GWAS Ctlg	rs2306986

GMAF

0.1267

Max Magnitude

0

?	(C;C) (C;G) (G;G)	28

[PMID 19878569] Candidate genetic analysis of plasma high-density lipoprotein-cholesterol and severity of coronary atherosclerosis.

ClinVar
Risk	rs2306986(C;C) rs2306986(T;T)
Alt	rs2306986(C;C) rs2306986(T;T)
Reference	Rs2306986(G;G)
Significance	Probable-non-pathogenic
Disease	Abetalipoproteinemia
Variation	info
Gene	MTTP
CLNDBN	Abetalipoproteinemia
Reversed	0
HGVS	NC_000004.11:g.100504575G>C
CLNSRC
CLNACC	RCV000276357.1,