Original source

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

Alleles
T/G|Ancestral: T|Ambiguity code: K|MAF: 0.23 (G)
Location

Chromosome 2:27136537 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

2:g.27136537T>G

About this variant

This variant overlaps 11 transcripts and has 2776 sample genotypes.

Variant displays