Most severe consequence
21
Intron variant
Alleles
C/T|Ancestral: C|MAF: 0.25 (T)|Highest population MAF: 0.45
Location
Chromosome 11:113296286 (forward strand)|View in location tab
Evidence status 
HGVS names
This variant has 7 HGVS names - Show
Synonyms
Archive dbSNP rs386515318, rs4134619, rs4986917, rs60979161, rs4646980, rs17294542
Genotyping chips
This variant has assays on 5 chips - Show
Original source
Variants (including SNPs and indels) imported from dbSNP (release 147)|View in dbSNP
About this variant
This variant overlaps 10 transcripts, has 3691 sample genotypes and is mentioned in 36 citations.
Description from SNPedia
Description not available [More information from SNPedia]