Original source

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

Alleles
TT/-|MAF: 0.45 (TT)
Location

Chromosome 6:143944784-143944785 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms
HGVS names

This variant has 17 HGVS names - Show

About this variant

This variant overlaps 19 transcripts and has 2508 sample genotypes.

Variant displays