Original source

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

Alleles
G/A|Ambiguity code: R
Location

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

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina BovineSNP50 BeadChip

About this variant

This variant overlaps 2 transcripts.

Variant displays