Original source

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

Alleles
G/T|Ancestral: G|Ambiguity code: K|MAF: 0.26 (T)
Location

Chromosome 17:15368756 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms
HGVS name

17:g.15368756G>T

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 1 transcript and has 3964 sample genotypes.

Variant displays