Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.03 (T)
Location

Chromosome 16:28877270 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

16:g.28877270C>T

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

Variant displays