Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

Chromosome 19:55151881 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM020190

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_113_TNNI3_191044_0004, 5855

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

About this variant

This variant overlaps 24 transcripts and is associated with 6 phenotypes.

Variant displays