Most severe consequence
28
intron variant
Alleles
A/G/T|Ancestral: G|Highest population MAF: 0.37
Change tolerance
CADD: G:1.660, T:1.425|GERP: -3.87
Location
Chromosome 22:18917482 (forward strand)|VCF:22 18917482 rs455135 A G,T
Evidence status 
HGVS names
This variant has 8 HGVS names - Show
Synonyms
This variant has 5 synonyms - Show
Genotyping chips
This variant has assays on: Affy GenomeWideSNP_6.0
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 and has 3009 sample genotypes.
