Most severe consequence
21
Intron variant
Alleles
A/G|Ancestral: A|MAF: 0.09 (G)|Highest population MAF: 0.23
Location
Chromosome 13:31873085 (forward strand)|View in location tab
Evidence status 
HGVS names
This variant has 2 HGVS names - Show
Synonyms
Archive dbSNP rs59296319, rs7336701, rs17076752
Genotyping chips
This variant has assays on: Affy GeneChip 500K, Affy GenomeWideSNP_6.0
Original source
Variants (including SNPs and indels) imported from dbSNP (release 149)|View in dbSNP
About this variant
This variant overlaps 1 transcript, has 3852 sample genotypes and is mentioned in 1 citation.
Description from SNPedia
Description not available [More information from SNPedia]
