Most severe consequence
28
intron variant
Alleles
C/A/G|Ancestral: C|MAF: 0.23 (G)|Highest population MAF: 0.49
Change tolerance
CADD: A:3.628, G:3.782|GERP: -1.66
Location
Chromosome 16:55684571 (forward strand)|VCF:16 55684571 rs12443955 C A,G
Evidence status 
HGVS names
This variant has 6 HGVS names - Show
Synonyms
This variant has 3 synonyms - Show
Genotyping chips
This variant has assays on 7 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 2 transcripts and has 3009 sample genotypes.
