Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCz10) (release 142) | View in dbSNP

Alleles
C/T | Ambiguity code: Y
Location

Chromosome 1:18855903 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 1 transcript and has 2 individual genotypes.

Variation displays