Most severe consequence
28
intron variant
Alleles
T/C/G|Ancestral: G|MAF: 0.24 (G)|Highest population MAF: 0.44
Change tolerance
CADD: C:7.900, G:7.496|GERP: -1.43
Location
Chromosome 6:35388863 (forward strand)|VCF:6 35388863 rs9658100 T C,G
Evidence status 
HGVS names
This variant has 8 HGVS names - Show
Synonyms
This variant has 3 synonyms - Show
Genotyping chips
This variant has assays on 9 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 3 transcripts, has 2504 sample genotypes and is mentioned in 1 citation.
