Most severe consequence
28
intron variant
Alleles
A/G|Ancestral: A|MAF: 0.09 (G)|Highest population MAF: 0.23
Change tolerance
CADD: G:1.304|GERP: -1.20
Location
Chromosome 5:159940268 (forward strand)|VCF:5 159940268 rs13162302 A G
Evidence status 
HGVS names
This variant has 2 HGVS names - Show
Synonyms
ClinGen Allele Registry CA12074492 (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, has 3009 sample genotypes and is mentioned in 3 citations.
Description from SNPedia
Description not available [More information from SNPedia]
