Most severe consequence
28
intron variant
Alleles
C/A/T|Ancestral: A|MAF: 0.48 (A)|Highest population MAF: 0.50
Change tolerance
CADD: A:0.492, T:0.810|GERP: -3.36
Location
Chromosome 5:37821119 (forward strand)|VCF:5 37821119 rs1549250 C A,T
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 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 1 transcript, has 3009 sample genotypes, is associated with 2 phenotypes and is mentioned in 10 citations.
