Original source

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

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

Chromosome 11:2129096 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

11:g.2129096G>A

About this variant

This variant overlaps 9 transcripts and has 2504 sample genotypes.

Variant displays