Most severe consequence
28
intron variant
Alleles
A/G|Ancestral: A|Highest population MAF: 0.46
Change tolerance
CADD: G:1.241
Location
Chromosome 1:66558759 (forward strand)|VCF:1 66558759 rs4655595 A G
Co-located variant
COSMIC COSV58471043
Evidence status 
HGVS names
This variant has 8 HGVS names - Show
Synonyms
This variant has 2 synonyms - Show
Genotyping chips
This variant has assays on 6 chips - Show
Original source
Variants (including SNPs and indels) imported from dbSNP (release 156)|View in dbSNP
About this variant
This variant overlaps 7 transcripts, has 2504 sample genotypes and is mentioned in 4 citations.
Description from SNPedia
rs4655595 has been reported in a large study to be associated with type-2 diabetes.... Show