Most severe consequence
21
Intron variant
Alleles
G/A|Ancestral: G|MAF: 0.32 (A)|Highest population MAF: 0.47
Location
Chromosome 11:133075651 (forward strand)|View in location tab
Evidence status 
HGVS names
This variant has 5 HGVS names - Show
Synonyms
Archive dbSNP rs57999851
Genotyping chips
This variant has assays on 10 chips - Show
Original source
Variants (including SNPs and indels) imported from dbSNP (release 149)|View in dbSNP
About this variant
This variant overlaps 2 transcripts and has 3683 sample genotypes.
