Most severe consequence
28
intron variant
Alleles
C/A/G/T|Ancestral: T|MAF: 0.15 (C)|Highest population MAF: 0.25
Change tolerance
CADD: A:0.359, G:0.369, T:0.456|GERP: -2.35
Location
Chromosome 11:18001867 (forward strand)|VCF:11 18001867 rs211134 C A,G,T
Evidence status 
HGVS names
This variant has 12 HGVS names - Show
Synonyms
This variant has 4 synonyms - Show
Genotyping chips
This variant has assays on: Affy GenomeWideSNP_6.0, Illumina_CytoSNP12v1
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.
