Original source

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

Alleles
TAA/-|MAF: 0.47 (-)
Location

Chromosome 20:58671478-58671480 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 23 transcripts and has 2508 sample genotypes.

Variant displays