Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 20:51788940 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM061189

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2009_August_001_069_SALL4_607343_0012, 14795

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

Variation displays