Most severe consequence
27
non coding transcript exon variant
Alleles
A/C/G/T|Ancestral: G|Highest population MAF: 0.43
Change tolerance
CADD: C:5.983, G:6.395, T:5.959|GERP: -3.43
Location
Chromosome 5:112892102 (forward strand)|VCF:5 112892102 rs712665 A C,G,T
Co-located variants
dbSNP rs746641681 (A/-) ; COSMIC COSV54839822
Evidence status 
HGVS names
This variant has 9 HGVS names - Show
Synonyms
This variant has 6 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 2 citations.
