Original source

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

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

Chromosome 6:34428027 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

6:g.34428027A>T

About this variant

This variant overlaps 8 transcripts.

Variant displays