Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.24 (A)

Chromosome 12:109807783 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs57379657, rs386546871

HGVS names

This variant has 10 HGVS names - Show

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant overlaps 8 transcripts, has 3693 sample genotypes and is mentioned in 1 citation.

Variant displays