Original source

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

-/T/TT | MAF: 0.18 (-)

Chromosome 12: between 20826230 and 20826231 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and has 2514 sample genotypes.

Variant displays