Most severe consequence
13
missense variant
Alleles
C/G|Highest population MAF: < 0.01
Location
Chromosome 3:19433076 (forward strand)|VCF:3 19433076 ENSVATH14424029 C G
HGVS names
This variant has 3 HGVS names - Show
External Links
About this variant
This variant overlaps 1 transcript and has 1106 sample genotypes.