Most severe consequence
28
intron variant
Alleles
G/A|Ancestral: G|Highest population MAF: 0.34
Change tolerance
CADD: A:16.24|GERP: 0.44
Location
Chromosome 5:94853029 (forward strand)|VCF:5 94853029 rs293032 G A
Co-located variant
COSMIC COSV56508757
Evidence status 
HGVS names
This variant has 3 HGVS names - Show
Synonyms
This variant has 7 synonyms - Show
Genotyping chips
This variant has assays on 7 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 2 transcripts, has 3009 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.
