Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 20:51789010 (forward strand) | View in location tab

Co-located

with COSMIC COSM1664030 (G/A) ; HGMD-PUBLIC CM022983

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2009_August_001_065_SALL4_607343_0005, 14788

This variation has 10 HGVS names - click the plus to show

Variation displays