Most severe consequence
28
intron variant
Alleles
G/A/C|Ancestral: A|MAF: 0.43 (A)|Highest population MAF: 0.50
Change tolerance
CADD: A:0.290, C:0.231|GERP: -1.60
Location
Chromosome 8:23250065 (forward strand)|VCF:8 23250065 rs12544038 G A,C
Evidence status 
HGVS names
This variant has 6 HGVS names - Show
Synonyms
This variant has 4 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 2 transcripts and has 3009 sample genotypes.
