Original source

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

Alleles
T/C/G|Ancestral: T|Ambiguity code: B
Location

Chromosome 8:142877221 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM970406

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 16798, 2010_April_001_011_CYP11B1_610613_0007

HGVS names

This variant has 18 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and is associated with 2 phenotypes.

Variant displays