Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 19:55663260 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM030288 ; PhenCode FHC0415 (C/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_115_TNNI3_191044_0006, 5857

This variation has 7 HGVS names - click the plus to show

Variation displays