Most severe consequence
28
intron variant
Alleles
G/A
Change tolerance
GERP: 0.91
Location
Primary_assembly 1:79999825 (forward strand)|VCF:1 79999825 rs13582785 G A
Evidence status 
HGVS names
This variant has 6 HGVS names - Show
Original source
Short variant data imported from EVA (release 4)|View in EVA
About this variant
This variant has predicted consequences for 5 transcripts.
