Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A | Ambiguity code: R | MAF: < 0.01 (A)
Location

Chromosome 11:356140 (forward strand) | View in location tab

Most severe consequence
 
TF binding site
HGVS name

11:g.356140G>A

About this variant

This variant overlaps 1 regulatory feature and has 2504 sample genotypes.

Variant displays