Original source

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

A/C | Ancestral: A | Ambiguity code: M | MAF: 0.36 (C)

Chromosome 16:23352760 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs152746, rs697218, rs3785360

HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 8 transcripts and has 3787 sample genotypes.

Variant displays