Most severe consequence
21
Intron variant
Alleles
G/A
Location
Chromosome 4:99729470 (forward strand)|View in location tab
Evidence status 
HGVS names
This variant has 2 HGVS names - Show
Genotyping chips
This variant has assays on: Illumina BovineSNP50 BeadChip
Original source
Variants (including SNPs and indels) imported from dbSNP (release 148)|View in dbSNP
About this variant
This variant overlaps 2 transcripts.
