Most severe consequence
28
intron variant
Alleles
T/A/G|Ancestral: A|MAF: 0.30 (T)|Highest population MAF: 0.49
Change tolerance
CADD: A:0.612, G:0.624|GERP: -2.95
Location
Chromosome 8:101989345 (forward strand)|VCF:8 101989345 rs4734051 T A,G
Evidence status 
HGVS names
This variant has 6 HGVS names - Show
Synonyms
This variant has 7 synonyms - Show
Genotyping chips
This variant has assays on: Affy GenomeWideSNP_6.0
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 and has 3009 sample genotypes.
