rs2322659

plus

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

Make rs2322659(C;C)

Make rs2322659(C;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

135798089

Gene

LCT

is a	snp
is	mentioned by
dbSNP	rs2322659
dbSNP (classic)	rs2322659
ClinGen	rs2322659
ebi	rs2322659
HLI	rs2322659
Exac	rs2322659
Gnomad	rs2322659
Varsome	rs2322659
LitVar	rs2322659
Map	rs2322659
PheGenI	rs2322659
Biobank	rs2322659
1000 genomes	rs2322659
hgdp	rs2322659
ensembl	rs2322659
geneview	rs2322659
scholar	rs2322659
google	rs2322659
pharmgkb	rs2322659
gwascentral	rs2322659
openSNP	rs2322659
23andMe	rs2322659
SNPshot	rs2322659
SNPdbe	rs2322659
MSV3d	rs2322659
GWAS Ctlg	rs2322659

GMAF

0.4885

Max Magnitude

0

?

(C;C) (C;T) (T;T)

28

[PMID 15114531 ] Genetic signatures of strong recent positive selection at the lactase gene.

[PMID 19326473 ] Natriuretic peptide system gene variants are associated with ventricular dysfunction after coronary artery bypass grafting.

[PMID 20017971 ] Assessing the impact of global versus local ancestry in association studies.

[PMID 20031626 ] Variation in the 4q25 chromosomal locus predicts atrial fibrillation after coronary artery bypass graft surgery.

[PMID 23420841 ] Genetic dissection of the preeclampsia susceptibility locus on chromosome 2q22 reveals shared novel risk factors for cardiovascular disease

ClinVar
Risk	rs2322659(C;C)
Alt	rs2322659(C;C)
Reference	Rs2322659(T;T)
Significance	Non-pathogenic
Disease	Congenital lactase deficiency Lactose intolerance
Variation	info
Gene	LCT
CLNDBN	Congenital lactase deficiency Lactose intolerance
Reversed	0
HGVS	NC_000002.11:g.136555659T>C
CLNSRC
CLNACC	RCV000349439.1, RCV000392923.1,