Most severe consequence
28
intron variant
Alleles
A/C/T|Ancestral: A|MAF: 0.34 (C)|Highest population MAF: 0.48
Change tolerance
CADD: C:0.853, T:0.818|GERP: -0.86
Location
Chromosome 5:36604099 (forward strand)|VCF:5 36604099 rs2562580 A C,T
Evidence status 
HGVS names
This variant has 4 HGVS names - Show
Synonyms
ClinGen Allele Registry CA16225114 (C), CA810267259 (T)
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 505 sample genotypes.
