Most severe consequence
21
intron variant
Alleles
C/T|Highest population MAF: 0.83
Location
Chromosome 3:335900365 (forward strand)|VCF:3 335900365 AX-93213911 C T
HGVS names
This variant has 5 HGVS names - Show
Original source
About this variant
This variant overlaps 4 transcripts and has 1351 sample genotypes.
