Original source

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

G/A | Ancestral: A | Ambiguity code: R | MAF: 0.19 (A)

Chromosome 17:7078660 (forward strand) | View in location tab

Most severe consequence
Non coding transcript exon variant
Evidence status


Archive dbSNP rs59779778

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 6 transcripts and has 3691 sample genotypes.

Variant displays