Original source

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

C/T | Ambiguity code: Y

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

Most severe consequence
Splice region variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 1 transcript and has 2 sample genotypes.

Variant displays