Most severe consequence
28
intron variant
Alleles
G/A/C/T|Ancestral: G|MAF: 0.35 (A)|Highest population MAF: 0.46
Change tolerance
CADD: A:2.314, C:0.783, T:0.795|GERP: -2.50
Location
Chromosome 8:101959951 (forward strand)|VCF:8 101959951 rs7839884 G A,C,T
Evidence status 
HGVS names
This variant has 9 HGVS names - Show
Synonyms
This variant has 5 synonyms - Show
Genotyping chips
This variant has assays on 5 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.
