Most severe consequence
28
intron variant
Alleles
G/A/T|Ancestral: T|MAF: 0.38 (T)|Highest population MAF: 0.50
Change tolerance
CADD: A:0.219, T:0.368|GERP: -1.95
Location
Chromosome 8:101974574 (forward strand)|VCF:8 101974574 rs1119377 G A,T
Evidence status 
HGVS names
This variant has 6 HGVS names - Show
Synonyms
This variant has 3 synonyms - Show
Genotyping chips
This variant has assays on 6 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 2 transcripts and has 3009 sample genotypes.
