Original source

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

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

Chromosome 20:967230 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM065447

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 16788, 2009_August_001_062_RSPO4_610573_0003

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

Variation displays