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 8:142879146 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM053826

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 16807, CYP11B1_281C_T_041511, 2010_April_001_014_CYP11B1_610613_0016

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 5 citations.

Variant displays