Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/A|Ancestral: G|Ambiguity code: R
Location

Chromosome 11:116790814 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM053767

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_017_APOA5_606368_0003, 13748

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 11 transcripts and is associated with 2 phenotypes.

Variant displays