Most severe consequence
28
intron variant
Alleles
A/C/G/T|Ancestral: G|MAF: 0.39 (A)|Highest population MAF: 0.50
Change tolerance
CADD: C:0.893, G:1.013, T:0.871|GERP: -3.25
Location
Chromosome 5:37817242 (forward strand)|VCF:5 37817242 rs2973050 A C,G,T
Evidence status 
HGVS names
This variant has 6 HGVS names - Show
Synonyms
This variant has 5 synonyms - Show
Genotyping chips
This variant has assays on 5 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 and is mentioned in 6 citations.
