Most severe consequence
40
intergenic variant
Alleles
G/C/T|Ancestral: G|MAF: 0.13 (C)|Highest population MAF: 0.43
Change tolerance
CADD: C:4.296, T:4.174|GERP: -1.28
Location
Chromosome 6:15664533 (forward strand)|VCF:6 15664533 rs2743852 G C,T
Evidence status 
HGVS names
This variant has 2 HGVS names - Show
Synonyms
ClinGen Allele Registry CA135268747 (C), CA821269042 (T)
Original source
Variants (including SNPs and indels) imported from dbSNP (release 156)|View in dbSNP
About this variant
This variant has 2504 sample genotypes and is mentioned in 8 citations.
