Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

Chromosome 11:116836271 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM990165

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_014_APOA1_107680_0024, 471

This variant has 15 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts, 2 regulatory features and is associated with 2 phenotypes.

Variant displays