Most severe consequence
21
Intron variant
Alleles
T/G|Highest population MAF: 0.26
Location
Chromosome 22:22365217 (forward strand)|View in location tab
Evidence status 
HGVS names
This variant has 2 HGVS names - Show
Original source
Variants (including SNPs and indels) imported from dbSNP (release 147)|View in dbSNP
About this variant
This variant overlaps 1 transcript and has 178 sample genotypes.
