Most severe consequence
21
intron variant
Alleles
G/A
Location
Chromosome 1:16148 (forward strand)|VCF:1 16148 rs5413863126 G A
HGVS names
This variant has 2 HGVS names - Show
External Links
Original source
EVA2024_rsID_mapped
About this variant
This variant overlaps 2 transcripts.
