Most severe consequence
12
Missense variant
Alleles
G/A|Ancestral: G
Location
Chromosome 22:45102568 (forward strand)|View in location tab
Evidence status 
HGVS names
This variant has 3 HGVS names - Show
Original source
Variants (including SNPs and indels) imported from dbSNP (release 136)|View in dbSNP
About this variant
This variant overlaps 1 transcript.
