Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.38 (A)
Location

Chromosome 20:22069865 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs60703434, rs58031434

This variant has 2 HGVS names - click the plus to show

20:g.22069865A>G
ENST00000449427.2:n.445+1177A>G

This variant has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 1 transcript, has 3966 sample genotypes, is associated with 1 phenotype and is mentioned in 3 citations.

Variant displays