Most severe consequence
12
Missense variant
Alleles
A/G|Ancestral: A|MAF: < 0.01 (G)|Highest population MAF: 0.05
Location
Chromosome 22:17735587 (forward strand)|View in location tab
Evidence status 
HGVS names
This variant has 36 HGVS names - Show
Synonyms
Uniprot VAR_061041
Genotyping chips
This variant has assays on: Illumina_HumanOmni1-Quad, Illumina_ExomeChip
Original source
Variants (including SNPs and indels) imported from dbSNP (release 149)|View in dbSNP
About this variant
This variant overlaps 23 transcripts and has 2505 sample genotypes.
