Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

A/T | Ancestral: T | Ambiguity code: W | MAF: 0.15 (A)

Chromosome 6:13246173 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs74290179

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Cardio-Metabo_Chip

About this variant

This variant overlaps 3 transcripts and has 2773 sample genotypes.

Variant displays