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 20:50407173 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM031725

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 14792, 2009_August_001_067_SALL4_607343_0009

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

Variation displays