Most severe consequence
28
intron variant
Alleles
A/G|Ancestral: G|MAF: 0.33 (G)|Highest population MAF: 0.50
Change tolerance
CADD: G:1.017|GERP: -3.01
Location
Chromosome 5:36603273 (forward strand)|VCF:5 36603273 rs2562578 A G
Evidence status 
HGVS names
This variant has 2 HGVS names - Show
Synonyms
ClinGen Allele Registry CA12168165 (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 1 transcript, 1 regulatory feature and has 3009 sample genotypes.
