Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057519093

From SNPedia

ClinVar
Risk rs1057519093(-;-)
Alt rs1057519093(-;-)
Reference Rs1057519093(GCTGGGCTCGAA;GCTGGGCTCGAA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene TNNI2
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.1862362_1862373delGCTGGGCTCGAA
CLNSRC
CLNACC RCV000415803.2,