Original source

Variants (including SNPs and indels) imported from dbSNP (release 145)|View in dbSNP

Alleles
C/T|Ambiguity code: Y
Location

Chromosome 1:302891339 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Pig SNP Consortium DBNP0000002

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_PorcineSNP60

About this variant

This variant overlaps 2 transcripts.

Variant displays