Original source

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

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

Chromosome 12:114398675 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM031376

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_127_TBX5_601620_0009, 10328

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

Variation displays