Most severe consequence
4
Stop gained
Alleles
G/A|Ancestral: G
Location
Chromosome 19:13277122 (forward strand)|View in location tab
Co-located variant
HGMD-PUBLIC CM983913
Evidence status 
Clinical significance
HGVS names
This variant has 49 HGVS names - Show
Synonyms
This variant has 2 synonyms - Show
Original source
Variants (including SNPs and indels) imported from dbSNP (release 149)|View in dbSNP
About this variant
This variant overlaps 21 transcripts, 2 regulatory features, is associated with 2 phenotypes and is mentioned in 1 citation.
Description from SNPedia
Description not available [More information from SNPedia]
