Original source

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

Alleles
G/C|Ancestral: G|Ambiguity code: S|MAF: 0.04 (C)
Location

Chromosome 20:58654779 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 22 HGVS names - Show

About this variant

This variant overlaps 21 transcripts and has 2505 sample genotypes.

Variant displays