Original source

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

Alleles
A/G|Ambiguity code: R|MAF: 0.47 (G)
Location

Chromosome 16:28483029 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 35 HGVS names - Show

About this variant

This variant overlaps 37 transcripts and has 2508 sample genotypes.

Variant displays