rs76863441

Orientation

plus

Stabilized

plus

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

Make rs76863441(A;A)

Make rs76863441(A;C)

Reference

GRCh38 38.1/141

Chromosome

6

Position

46709361

Gene

PLA2G7

is a	snp
is	mentioned by
dbSNP	rs76863441
dbSNP (classic)	rs76863441
ClinGen	rs76863441
ebi	rs76863441
HLI	rs76863441
Exac	rs76863441
Gnomad	rs76863441
Varsome	rs76863441
LitVar	rs76863441
Map	rs76863441
PheGenI	rs76863441
Biobank	rs76863441
1000 genomes	rs76863441
hgdp	rs76863441
ensembl	rs76863441
geneview	rs76863441
scholar	rs76863441
google	rs76863441
pharmgkb	rs76863441
gwascentral	rs76863441
openSNP	rs76863441
23andMe	rs76863441
SNPshot	rs76863441
SNPdbe	rs76863441
MSV3d	rs76863441
GWAS Ctlg	rs76863441

Merged from

Rs16874954

GMAF

0.02984

Max Magnitude

0

OMIM	601690
Desc
Variant	0001
Related	also

ClinVar
Risk	rs76863441(A;A)
Alt	rs76863441(A;A)
Reference	Rs76863441(C;C)
Significance	Pathogenic
Disease	Platelet-activating factor acetylhydrolase deficiency
Variation	info
Gene	PLA2G7
CLNDBN	Platelet-activating factor acetylhydrolase deficiency
Reversed	0
HGVS	NC_000006.11:g.46677098C>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000008376.3,

?	(A;A) (A;C) (C;C)

[PMID 23404648] An association study between genetic polymorphisms related to lipoprotein-associated phospholipase A(2) and coronary heart disease.