Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W | MAF: 0.11 (A)
Location

Chromosome 11:128858172 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts, has 2539 sample genotypes and is mentioned in 1 citation.

Variant displays