Most severe consequence
21
Intron variant
Alleles
T/G
Location
Chromosome 8:45589154 (forward strand)|View in location tab
HGVS names
This variant has 2 HGVS names - Show
Original source
Variants (including SNPs and indels) imported from dbSNP (release 148)|View in dbSNP
About this variant
This variant overlaps 1 transcript.
