Original source

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

Alleles
G/T|Ancestral: T|Ambiguity code: K|MAF: 0.02 (T)
Location

Chromosome 2:192748268 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

2:g.192748268G>T

About this variant

This variant overlaps 2 transcripts and has 2768 sample genotypes.

Variant displays