Most severe consequence
28
intron variant
Alleles
G/A/C/T|Ancestral: T|MAF: 0.40 (T)|Highest population MAF: 0.49
Change tolerance
CADD: A:7.129, C:4.833, T:4.849|GERP: -0.30
Location
Chromosome 14:73330961 (forward strand)|VCF:14 73330961 rs12435797 G A,C,T
Evidence status 
HGVS names
This variant has 27 HGVS names - Show
Synonyms
This variant has 5 synonyms - Show
Genotyping chips
This variant has assays on 8 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 8 transcripts, has 3009 sample genotypes, is associated with 1 phenotype and is mentioned in 4 citations.
Description from SNPedia
Description not available [More information from SNPedia]
