Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.05 (A)
Location

Chromosome 20:6766559 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

20:g.6766559G>A

About this variant

This variant overlaps 1 transcript and has 2506 sample genotypes.

Variant displays