Original source

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

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

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

Co-located variant

HGMD-PUBLIC CM990165

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_014_APOA1_107680_0024, 471

HGVS names

This variant has 15 HGVS names - Show

About this variant

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

Variant displays