Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W | MAF: 0.11 (A)
Location

Chromosome 16:47664805 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

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

About this variant

Variant displays