Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

C/T | Ancestral: C | Ambiguity code: Y

Chromosome 20:762230 (forward strand) | View in location tab

Most severe consequence
Intron variant
HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 270 sample genotypes.

Variant displays