Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.48 (T)
Location

Chromosome 16:2278649 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 4 HGVS names - click the plus to show

This variant has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts, 1 regulatory feature, has 3798 sample genotypes and is mentioned in 2 citations.

Variant displays