Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S
Location

Chromosome 22:19764224 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM071113

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 10751, 2009_August_001_104_TBX1_602054_0005

This variation has 12 HGVS names - click the plus to show

Variation displays