Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
C/T|Ancestral: C|Ambiguity code: Y
Location

Chromosome 17:61456674 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM041450

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 10463, 2010_April_001_218_TBX4_601719_0002

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature and is associated with 2 phenotypes.

Variant displays