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 8:142879690 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM970405

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB CYP11B1_124C_T_020111, 16800, 2010_April_001_013_CYP11B1_610613_0009

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 6 transcripts, is associated with 3 phenotypes and is mentioned in 6 citations.

Variant displays