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 20:968000 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM065446

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 16789, 2009_August_001_063_RSPO4_610573_0004

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

Variation displays