Original source

Variants (including SNPs and indels) imported from dbSNP (release 140) | [View in dbSNP]

Alleles
T/G | Ambiguity code: K
Location

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

Most severe consequence
Synonyms

NextGen Project ss1142502571, ss1204545153, ss1219569927

HGVS name

19:g.11662409T>G

Genotyping chips

This variation has assays on: IlluminaOvineHDSNP

About this variant

This variant overlaps 1 transcript and has 194 individual genotypes.

Variation displays