Original source

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

A/C/T | Ancestral: A | Ambiguity code: H | MAF: 0.19 (C)

Chromosome 16:28904112 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs2234849

HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 16 transcripts and has 3687 sample genotypes.

Variant displays