Original source

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

Clinical significance

Synonyms

LSDB 2010_April_001_111_TNNI3_191044_0002, 5853

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

Variation displays