Most severe consequence
28
intron variant
Alleles
G/A|Ancestral: G|MAF: 0.28 (A)|Highest population MAF: 0.49
Change tolerance
CADD: A:0.154
Location
Chromosome 6:15658674 (forward strand)|VCF:6 15658674 rs1997679 G A
Evidence status 
HGVS names
This variant has 4 HGVS names - Show
Synonyms
This variant has 2 synonyms - Show
Genotyping chips
This variant has assays on 9 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, 1 regulatory feature, has 2504 sample genotypes and is mentioned in 12 citations.
