This variation has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
T/A/C/G | Ancestral: T | Ambiguity code: N
Location

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

Co-located

with HGMD-PUBLIC CM970406

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 16798, 2010_April_001_011_CYP11B1_610613_0007

This variation has 27 HGVS names - click the plus to show

About this variant

This variant overlaps 18 transcripts and is associated with 2 phenotypes.

Variation displays