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
 
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