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
HGVS name

19:g.11662409T>G

Genotyping chips

This variation has assays on: IlluminaOvineHDSNP

Variation displays