Most severe consequence
28
intron variant
Alleles
A/C|Ancestral: A|MAF: 0.38 (C)|Highest population MAF: 0.49
Change tolerance
CADD: C:7.498|GERP: -1.70
Location
Chromosome 8:101935440 (forward strand)|VCF:8 101935440 rs13278642 A C
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: Illumina_HumanOmni5, Illumina_HumanOmni2.5
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.
