Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 10751, 2009_August_001_104_TBX1_602054_0005

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

About this variant

This variant overlaps 7 transcripts and is associated with 2 phenotypes.

Variant displays