List of variants in gene TTN reported as likely benign by Blueprint Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.104560G>C (p.Val34854Leu)	rs55866005	0.00531
NM_001267550.2(TTN):c.26863A>G (p.Ile8955Val)	rs72648994	0.00274
NM_001267550.2(TTN):c.44281C>T (p.Pro14761Ser)	rs192766485	0.00057
NM_001267550.2(TTN):c.63589A>G (p.Ile21197Val)	rs72646855	0.00054
NM_001267550.2(TTN):c.64072G>A (p.Val21358Met)	rs371725212	0.00002
NM_001267550.2(TTN):c.15500C>A (p.Pro5167His)	rs730880237
NM_001267550.2(TTN):c.3002T>C (p.Met1001Thr)	rs148269839

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