Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome 19:55151851 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM971500 ; PhenCode FHC0423 (T/G)

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 5853, 2010_April_001_111_TNNI3_191044_0002

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

About this variant

This variant overlaps 24 transcripts and is associated with 3 phenotypes.

Variant displays