Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.42 (G)

Chromosome 11:46843449 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs17790006

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 3759 sample genotypes.

Variant displays