Most severe consequence
38
Intergenic variant
Alleles
T/C|Highest population MAF: 0.48
Location
Chromosome 18:64249211 (forward strand)|View in location tab
Evidence status 
HGVS name
NC_019475.1:g.64249211T>C
Original source
Variants (including SNPs and indels) imported from dbSNP (release 147)|View in dbSNP
About this variant
This variant has 180 sample genotypes.
