Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 20:59321127 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM960505

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 1709, 2009_August_001_008_EDN3_131242_0002

This variation has 11 HGVS names - click the plus to show

Variation displays