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
| See all predicted consequences [Genes and regulation]
Evidence status

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

About this variant

This variant overlaps 7 transcripts and has 2896 individual genotypes.

Variation displays