Original source

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

T/G | Ambiguity code: K

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

Most severe consequence
Downstream gene variant
Evidence status

HGVS name


Genotyping chips

This variant has assays on: IlluminaOvineHDSNP

About this variant

This variant overlaps 1 transcript and has 180 sample genotypes.

Variant displays