Original source

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

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

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