Most severe consequence
21
Intron variant
Alleles
C/T|Ancestral: C|MAF: 0.13 (T)|Highest population MAF: 0.25
Location
Chromosome 7:24967101 (forward strand)|View in location tab
Evidence status 
HGVS names
This variant has 7 HGVS names - Show
Synonyms
Archive dbSNP rs60121076
Genotyping chips
This variant has assays on 7 chips - Show
Original source
Variants (including SNPs and indels) imported from dbSNP (release 149)|View in dbSNP
About this variant
This variant overlaps 2 transcripts and has 3761 sample genotypes.
