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 4:110621210 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM981540

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 23129, 2010_April_001_061_PITX2_601542_0012

This variation has 22 HGVS names - click the plus to show

Variation displays