Most severe consequence
28
intron variant
Alleles
G/A|Ancestral: G|MAF: 0.05 (A)|Highest population MAF: 0.25
Change tolerance
CADD: A:1.769|GERP: -0.09
Location
Chromosome 18:2865507 (forward strand)|VCF:18 2865507 rs28877609 G A
Evidence status 
HGVS names
This variant has 2 HGVS names - Show
Synonyms
ClinGen Allele Registry CA295491229 (A)
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, has 2504 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.
Description from SNPedia
Description not available [More information from SNPedia]
