Most severe consequence
38
Intergenic variant
Alleles
A/T|Highest population MAF: 0.50
Location
Chromosome 13:2920437 (forward strand)|View in location tab
Evidence status 
HGVS name
NC_006100.4:g.2920437A>T
Original source
Variants (including SNPs and indels) imported from dbSNP (release 147)|View in dbSNP
About this variant
This variant has 4 sample genotypes.
