Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.48 (G)

Chromosome 3:184378790 (forward strand) | View in location tab


with HGMD-PUBLIC CR084015

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs57526857, rs386619456

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 20 transcripts, 1 regulatory feature, has 3795 sample genotypes and is mentioned in 1 citation.

Variant displays