Most severe consequence
28
intron variant
Alleles
G/A/C|Ancestral: A|MAF: 0.31 (G)|Highest population MAF: 0.49
Change tolerance
CADD: A:7.364, C:6.929|GERP: -0.84
Location
Chromosome 8:102009675 (forward strand)|VCF:8 102009675 rs4734610 G A,C
Evidence status 
HGVS names
This variant has 6 HGVS names - Show
Synonyms
This variant has 4 synonyms - 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 2 transcripts and has 3009 sample genotypes.
