Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

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

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

Co-located

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

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_114_TNNI3_191044_0005, 5856

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

Variation displays