Most severe consequence
28
intron variant
Alleles
T/A/G|Ancestral: T|MAF: 0.49 (T)|Highest population MAF: 0.50
Change tolerance
CADD: A:1.102, G:1.145|GERP: -2.96
Location
Chromosome 5:153803165 (forward strand)|VCF:5 153803165 rs1461225 T A,G
Evidence status 
HGVS names
This variant has 8 HGVS names - Show
Synonyms
This variant has 3 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, has 3009 sample genotypes, is associated with 1 phenotype and is mentioned in 5 citations.
