Original source

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

Alleles
C/A/T | Ancestral: C | Ambiguity code: H | MAF: < 0.01 (T)
Location

Chromosome 20:59321158 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM010833

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2009_August_001_011_EDN3_131242_0007, 1714

This variation has 17 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts, has 2504 individual genotypes and is associated with 2 phenotypes.

Variation displays