Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.01 (A)

Chromosome 3:170995925 (forward strand) | View in location tab

Most severe consequence
Upstream gene variant
Evidence status

HGVS name


Genotyping chips

This variant has assays on: Illumina_Cardio-Metabo_Chip

About this variant

This variant overlaps 4 transcripts and has 2504 sample genotypes.

Variant displays