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

IllumniaOvineHDSNP oar3_OAR19_11662409

HGVS name

19:g.11662409T>G

Genotyping chips

This variation has assays on: IlluminaOvineHDSNP

Variation displays