Most severe consequence
21
Intron variant
Alleles
C/T
Location
Chromosome 18:49080803 (forward strand)|View in location tab
HGVS names
This variant has 4 HGVS names - Show
Original source
Variants (including SNPs and indels) imported from dbSNP (release 146)|View in dbSNP
About this variant
This variant overlaps 3 transcripts.
