Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome 4:110621214 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM961113

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_056_PITX2_601542_0003, 10228

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

Variation displays