Original source

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

Alleles
A/-|Ancestral: A
Location

Chromosome 20:53566987 (forward strand)|View in location tab

Co-located variant

dbSNP rs74838016 (A/C)

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 7 sample genotypes.

Variant displays