Original source

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

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

Chromosome 11:3825566 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant

This variant has 19 HGVS names - click the plus to show

About this variant

This variant overlaps 41 transcripts and 1 regulatory feature.

Variant displays