Most severe consequence
 
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

About this variant

This variant overlaps 4 transcripts and has 1351 sample genotypes.

Variant displays