Original source

Variants (including SNPs and indels) imported from dbSNP (release 143) | View in dbSNP

G/A | Ambiguity code: R

Chromosome 4:99729470 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

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

Genotyping chips

This variant has assays on: Illumina BovineSNP50 BeadChip

About this variant

This variant overlaps 2 transcripts.

Variant displays