Original source

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

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

Chromosome 8:142876242 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM980494, CM930175

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 16794, 2010_April_001_008_CYP11B1_610613_0003

This variant has 9 HGVS names - click the plus to show

About this variant

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

Variant displays