Original source

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

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

Chromosome 19:55151898 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM030530 ; PhenCode FHC0414 (T/C)

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_114_TNNI3_191044_0005, 5856

HGVS names

This variant has 10 HGVS names - Show

About this variant

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

Variant displays