Original source

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

Alleles
T/A|Ancestral: A|Ambiguity code: W|MAF: 0.14 (A)
Location

Chromosome 17:7080816 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms
HGVS name

17:g.7080816T>A

About this variant

This variant overlaps 6 transcripts and has 2848 sample genotypes.

Variant displays