Most severe consequence
28
intron variant
Alleles
T/A/C/G|Ancestral: G|MAF: 0.29 (T)|Highest population MAF: 0.42
Change tolerance
CADD: A:2.507, C:2.768, G:2.505|GERP: -0.83
Location
Chromosome 5:112861940 (forward strand)|VCF:5 112861940 rs712668 T A,C,G
Evidence status 
HGVS names
This variant has 9 HGVS names - Show
Synonyms
ClinGen Allele Registry CA1573530021 (A), CA1573530022 (C), CA12007549 (G)
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, 1 regulatory feature and has 3009 sample genotypes.
