Original source

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

A/G | Ambiguity code: R

Chromosome 8:108833985 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 2 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina BovineHD BeadChip

About this variant

This variant overlaps 1 transcript and has 8 individual genotypes.

Variation displays