Most severe consequence
28
intron variant
Alleles
T/A/C/G|Ancestral: T|MAF: 0.33 (C)|Highest population MAF: 0.49
Change tolerance
CADD: A:7.574, C:7.898, G:7.544|GERP: -2.29
Location
Chromosome 14:73281790 (forward strand)|VCF:14 73281790 rs8013402 T A,C,G
Evidence status 
HGVS names
This variant has 27 HGVS names - Show
Synonyms
This variant has 4 synonyms - Show
Genotyping chips
This variant has assays on 7 chips - Show
Original source
Variants (including SNPs and indels) imported from dbSNP (release 156)|View in dbSNP
About this variant
This variant has predicted consequences for 8 transcripts and has 3009 sample genotypes.
