Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 6:1611721 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Evidence status

This variant has 3 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 1 transcript and 2 regulatory features.

Variant displays