Original source

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

Alleles
TGT/- | MAF: 0.12 (TGT)
Location

Chromosome 11:45961640-45961642 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

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

About this variant

This variant overlaps 4 transcripts and has 2513 sample genotypes.

Variant displays