Original source

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

A/C | Ancestral: C | Ambiguity code: M | MAF: 0.24 (A)

Chromosome 12:109816652 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs58784677

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 9 transcripts and has 2509 sample genotypes.

Variant displays