Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.31 (G)
Location

Chromosome 16:28487970 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 38 HGVS names - click the plus to show

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 42 transcripts and has 3697 sample genotypes.

Variant displays