Original source

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

G/T | Ancestral: G | Ambiguity code: K

Chromosome 6:143968876 (forward strand) | View in location tab

Most severe consequence
Non coding transcript exon variant
HGVS names

This variant has 20 HGVS names - Show

About this variant

This variant overlaps 21 transcripts and 1 regulatory feature.

Variant displays