Most severe consequence
40
intergenic variant
Alleles
A/G/T|Ancestral: A|MAF: 0.30 (G)|Highest population MAF: 0.49
Change tolerance
CADD: G:0.042, T:0.032|GERP: -1.73
Location
Chromosome 5:145317926 (forward strand)|VCF:5 145317926 rs10515549 A G,T
Evidence status 
HGVS names
This variant has 2 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 3009 sample genotypes and is mentioned in 1 citation.
