Most severe consequence
28
intron variant
Alleles
T/G|Ancestral: T|Highest population MAF: 0.47
Change tolerance
CADD: G:11.40
Location
Chromosome 8:116583551 (forward strand)|VCF:8 116583551 rs1028274 T G
Evidence status 
HGVS names
This variant has 6 HGVS names - Show
Synonyms
This variant has 4 synonyms - Show
Original source
Variants (including SNPs and indels) imported from dbSNP (release 156)|View in dbSNP
About this variant
This variant overlaps 5 transcripts, has 2504 sample genotypes and is associated with 1 phenotype.