Original source

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

Alleles
-/T | MAF: 0.42 (-)
Location

Chromosome 11: between 112037778 and 112037779 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

This variant has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 2506 sample genotypes.

Variant displays