Most severe consequence
12
Missense variant
Alleles
G/A|Ancestral: G|MAF: < 0.01 (A)|Highest population MAF: 0.03
Location
Chromosome 1:150578851 (forward strand)|View in location tab
Evidence status 
HGVS names
This variant has 13 HGVS names - Show
Synonyms
Uniprot VAR_024022
Genotyping chips
This variant has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni5, Illumina_ExomeChip
Original source
Variants (including SNPs and indels) imported from dbSNP (release 149)|View in dbSNP
About this variant
This variant overlaps 5 transcripts, 1 regulatory feature and has 2590 sample genotypes.
Description from SNPedia
Description not available [More information from SNPedia]
