Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.03 (G)
Location

Chromosome 20:6766908 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs59349630

HGVS name

20:g.6766908A>G

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 1 transcript and has 3626 sample genotypes.

Variant displays