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 12:114385521 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM971438

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 10322, 2010_April_001_122_TBX5_601620_0003

This variation has 9 HGVS names - click the plus to show

Variation displays