Original source

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

G/A | Ancestral: A | Ambiguity code: R | MAF: 0.03 (G)

Chromosome 1:20649722 (forward strand) | View in location tab

Most severe consequence
Non coding transcript exon variant
Evidence status

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and has 2513 sample genotypes.

Variant displays