Most severe consequence
28
intron variant
Alleles
C/A|Ancestral: C|MAF: 0.43 (A)|Highest population MAF: 0.45
Change tolerance
CADD: A:7.296|GERP: -2.96
Location
Chromosome 4:90907222 (forward strand)|VCF:4 90907222 rs11097273 C A
Evidence status 
HGVS names
This variant has 2 HGVS names - Show
Synonyms
This variant has 3 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 1 transcript and has 3009 sample genotypes.
