Original source

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

T/A | Ancestral: T | Ambiguity code: W

Chromosome 17:75132140 (forward strand) | View in location tab

Most severe consequence
Non coding transcript exon variant
HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 28 transcripts and 1 regulatory feature.

Variant displays