List of variants in gene combination LOC126806421, TTN reported as uncertain significance by Illumina Laboratory Services, Illumina

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.96501T>C (p.Ser32167=)	rs139223781	0.00251
NM_001267550.2(TTN):c.96918C>T (p.Ile32306=)	rs72648266	0.00064
NM_001267550.2(TTN):c.96234C>T (p.Tyr32078=)	rs376532382	0.00018
NM_001267550.2(TTN):c.96252A>G (p.Thr32084=)	rs369626133	0.00018
NM_001267550.2(TTN):c.96173G>A (p.Arg32058Gln)	rs374063064	0.00014
NM_001267550.2(TTN):c.96904+4T>C	rs373514079	0.00014
NM_001267550.2(TTN):c.96592C>G (p.Leu32198Val)	rs752075170	0.00001
NM_001267550.2(TTN):c.96931A>G (p.Met32311Val)	rs727504981	0.00001
NM_001267550.2(TTN):c.96235G>A (p.Asp32079Asn)	rs200540781
NM_001267550.2(TTN):c.96491A>G (p.Tyr32164Cys)	rs886055229

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