Most severe consequence
28
intron variant
Alleles
G/A/C|Ancestral: G|MAF: 0.32 (G)|Highest population MAF: 0.50
Change tolerance
CADD: A:11.77, C:11.28|GERP: -1.86
Location
Chromosome 5:112836522 (forward strand)|VCF:5 112836522 rs411356 G A,C
Evidence status 
Clinical significance
HGVS names
This variant has 16 HGVS names - Show
Synonyms
This variant has 4 synonyms - Show
Genotyping chips
This variant has assays on 5 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 7 transcripts, has 3009 sample genotypes, is associated with 2 phenotypes and is mentioned in 1 citation.
