Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and has 2514 sample genotypes.

Variant displays