Original source

Variants (including SNPs and indels) imported from dbSNP (release 140) | View in dbSNP

Alleles
A/T | Ambiguity code: W
Location

Chromosome 13:2290337 (forward strand) | View in location tab

Most severe consequence
 
Intergenic variant
Evidence status

HGVS name

13:g.2290337A>T

About this variant

This variant has 4 sample genotypes.

Variant displays