Most severe consequence
28
intron variant
Alleles
G/A|Ancestral: G|MAF: 0.31 (G)|Highest population MAF: 0.49
Change tolerance
CADD: A:0.620|GERP: -2.34
Location
Chromosome 8:101992630 (forward strand)|VCF:8 101992630 rs7829974 G A
Evidence status 
HGVS names
This variant has 3 HGVS names - Show
Synonyms
This variant has 3 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, 1 regulatory feature and has 3009 sample genotypes.
