Original source

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

HGMD-PUBLIC CM010833

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 1714, 2009_August_001_011_EDN3_131242_0007

HGVS names

This variant has 22 HGVS names - Show

About this variant

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

Variant displays