Most severe consequence
28
intron variant
Alleles
G/C/T|Ancestral: T|MAF: 0.50 (T)|Highest population MAF: 0.49
Change tolerance
CADD: C:0.888, T:0.850|GERP: -3.53
Location
Chromosome 21:40055397 (forward strand)|VCF:21 40055397 rs2837399 G C,T
Evidence status 
HGVS names
This variant has 4 HGVS names - Show
Synonyms
This variant has 6 synonyms - Show
Genotyping chips
This variant has assays on: Affy GenomeWideSNP_6.0, Affy GeneChip 500K
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 and has 3009 sample genotypes.
