Most severe consequence
28
intron variant
Alleles
G/A/T|Ancestral: T|Highest population MAF: 0.34
Change tolerance
CADD: A:1.831, T:1.183|GERP: -2.94
Location
Chromosome 15:55498112 (forward strand)|VCF:15 55498112 rs3743204 G A,T
Co-located variant
COSMIC COSV58249893
Evidence status 
Clinical significance
HGVS names
This variant has 12 HGVS names - Show
Synonyms
This variant has 4 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 5 transcripts, has 3009 sample genotypes, is associated with 1 phenotype and is mentioned in 19 citations.
