Most severe consequence
28
intron variant
Alleles
A/G/T|Ancestral: G|MAF: 0.49 (A)|Highest population MAF: 0.50
Change tolerance
CADD: G:0.856, T:0.740|GERP: -4.03
Location
Chromosome 5:45285650 (forward strand)|VCF:5 45285650 rs16902086 A G,T
Evidence status 
HGVS names
This variant has 4 HGVS names - Show
Synonyms
ClinGen Allele Registry CA12051803 (G), CA1543608793 (T)
Genotyping chips
This variant has assays on 6 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 1 phenotype and is mentioned in 4 citations.
