Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 8:142875730 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM062570

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 16808, 2010_April_001_015_CYP11B1_610613_0017

This variant has 11 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts and is associated with 2 phenotypes.

Variant displays