Most severe consequence
26
3 prime UTR variant
Alleles
G/A/C/T|Ancestral: G|Highest population MAF: 0.49
Change tolerance
CADD: A:10.37, C:9.800, T:9.584|GERP: -1.65
Location
Chromosome 5:175441697 (forward strand)|VCF:5 175441697 rs686 G A,C,T
Co-located variants
COSMIC COSV67104358 ; HGMD-PUBLIC CR082013
Evidence status 
HGVS names
This variant has 9 HGVS names - Show
Synonyms
This variant has 8 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 and is mentioned in 91 citations.
