Original source

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

Alleles
T/G | Ambiguity code: K
Location

Chromosome 19:11662409 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

19:g.11662409T>G

Genotyping chips

This variant has assays on: IlluminaOvineHDSNP

About this variant

This variant overlaps 1 transcript and has 180 sample genotypes.

Variant displays