Original source

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

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

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

Co-located variants

HGMD-PUBLIC CM980494, CM930175

Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB 16794, 2010_April_001_008_CYP11B1_610613_0003

HGVS names

This variant has 9 HGVS names - Show

About this variant

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

Variant displays