Most severe consequence
28
intron variant
Alleles
C/A/G|Ancestral: C|MAF: 0.35 (G)|Highest population MAF: 0.50
Change tolerance
CADD: A:4.394, G:4.573|GERP: 0.18
Location
Chromosome 8:23244230 (forward strand)|VCF:8 23244230 rs7459962 C A,G
Evidence status 
HGVS names
This variant has 22 HGVS names - Show
Synonyms
This variant has 3 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 1 transcript, has 3009 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.
