Original source

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

This variant has assays on 7 chips - click the plus to show

About this variant

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

Variant displays