Most severe consequence
38
Intergenic variant
Alleles
G/C|Highest population MAF: < 0.01
Location
Chromosome 2L:145 (forward strand)|View in location tab
HGVS name
NT_033779.5:g.145G>C
Original source
Variation features from DPGP, with Ensembl identifiers (release 1)|DPGP 1
About this variant
This variant has 1 sample genotype.
