Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 16:3592798 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Archive dbSNP rs3169470

This variant has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 2 sample genotypes.

Variant displays