Most severe consequence
21
intron variant
Alleles
A/T
Location
Chromosome 1:1879 (forward strand)|VCF:1 1879 rs5413865353 A T
HGVS names
This variant has 2 HGVS names - Show
External Links
Original source
EVA2024_rsID_mapped
About this variant
This variant overlaps 1 transcript.
