Most severe consequence
28
intron variant
Alleles
C/A/G|Ancestral: C|MAF: 0.24 (G)|Highest population MAF: 0.48
Change tolerance
CADD: A:5.492, G:5.127|GERP: 0.30
Location
Chromosome 16:55690565 (forward strand)|VCF:16 55690565 rs2397772 C A,G
Evidence status 
HGVS names
This variant has 6 HGVS names - Show
Synonyms
ClinGen Allele Registry CA721903437 (A), CA281417081 (G)
Genotyping chips
This variant has assays on 4 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, has 3009 sample genotypes and is mentioned in 1 citation.
