Most severe consequence
 
Missense variant
Alleles
T/C|MAF: 0.05 (C)|Highest population MAF: 0.35
Location

Chromosome 6:160540105 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM074331

Evidence status

HGVS names

This variant has 5 HGVS names - Show

Synonyms

This variant has 2 synonyms - Show

Genotyping chips

This variant has assays on 6 chips - Show

Original source

Variants (including SNPs and indels) imported from dbSNP (release 149)|View in dbSNP

About this variant

This variant overlaps 1 transcript, has 3099 sample genotypes, is associated with 1 phenotype and is mentioned in 73 citations.

Description from SNPedia

rs3798220, also known as I4399M or Ile4399Met, is a SNP in the apolipoprotein(A) LPA gene that has been reported to be associated with elevated plasma lipoprotein(a) [Lp(a)] and increased cardiovascular risk, and in particular, coronary artery disease.... Show

Variant displays