Most severe consequence
12
Missense variant
Alleles
G/A|Ancestral: G
Location
Chromosome 18:60371694 (forward strand)|View in location tab
Co-located variant
HGMD-PUBLIC CM050063
Evidence status 
Clinical significance
HGVS names
This variant has 5 HGVS names - Show
Synonyms
This variant has 4 synonyms - Show
Original source
Variants (including SNPs and indels) imported from dbSNP (release 149)|View in dbSNP
About this variant
This variant overlaps 1 transcript and is associated with 3 phenotypes.
Description from SNPedia
Description not available [More information from SNPedia]
