Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 20:50407068 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM022667

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 14784, 2009_August_001_064_SALL4_607343_0001

This variation has 5 HGVS names - click the plus to show

Variation displays