Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W
Location

Chromosome 20:50408499 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM031724

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 14791, 2009_August_001_066_SALL4_607343_0008

This variation has 6 HGVS names - click the plus to show

Variation displays