Original source

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

Alleles
G/-|Ancestral: G|MAF: 0.44 (G)
Location

Chromosome 12:20820796 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 2509 sample genotypes.

Variant displays