Original source

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

Alleles
T/G | Ancestral: G | Ambiguity code: K | MAF: 0.22 (T)
Location

Chromosome 20:766241 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
| See all predicted consequences [Genes and regulation]
Evidence status

Synonyms

Archive dbSNP rs57849739

This variation has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 3110 individual genotypes.

Variation displays