Original source

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

Alleles
A/G|Ancestral: T|Ambiguity code: R|MAF: 0.18 (G)
Location

Chromosome 20:6766960 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs61728311, rs61168936

HGVS name

20:g.6766960A>G

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 1 transcript, has 3967 sample genotypes and is mentioned in 2 citations.

Variant displays