Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.04 (G)

Chromosome 11:46720939 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Cardio-Metabo_Chip, Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 5 transcripts and has 2550 sample genotypes.

Variant displays