Most severe consequence
28
intron variant
Alleles
A/G|MAF: 0.13 (A)|Highest population MAF: 0.28
Change tolerance
CADD: G:1.690|GERP: -1.89
Location
Chromosome 6:35418264 (forward strand)|VCF:6 35418264 rs9462082 A G
Evidence status 
HGVS names
This variant has 4 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 3 transcripts, has 2504 sample genotypes and is mentioned in 5 citations.
