Most severe consequence
28
intron variant
Alleles
A/G|Ancestral: A|MAF: 0.09 (G)|Highest population MAF: 0.31
Change tolerance
CADD: G:1.373|GERP: -0.27
Location
Chromosome 6:35354986 (forward strand)|VCF:6 35354986 rs7744392 A G
Evidence status 
HGVS names
This variant has 4 HGVS names - Show
Synonyms
This variant has 2 synonyms - Show
Genotyping chips
This variant has assays on 10 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, is associated with 1 phenotype and is mentioned in 4 citations.
Description from SNPedia
Description not available [More information from SNPedia]
