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 16:89689495 (forward strand)|View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs386569965, rs57123318

HGVS names

This variant has 18 HGVS names - Show

Genotyping chips

This variant has assays on 15 chips - Show

About this variant

This variant overlaps 24 transcripts, has 4000 sample genotypes, is associated with 4 phenotypes and is mentioned in 12 citations.

Variant displays