Original source

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

TGT/- | MAF: 0.12 (TGT)

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

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 2513 sample genotypes.

Variant displays