List of variants in gene combination LOC126806425, TTN reported by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.52917T>C (p.Asp17639=)	rs73036398	0.02352
NM_001267550.2(TTN):c.52706-17A>G	rs72646807	0.01524
NM_001267550.2(TTN):c.53192T>C (p.Ile17731Thr)	rs72646809	0.01131
NM_001267550.2(TTN):c.53096G>A (p.Arg17699His)	rs72646808	0.00118
NM_001267550.2(TTN):c.52852C>T (p.Arg17618Cys)	rs201213901	0.00115
NM_001267550.2(TTN):c.52891G>A (p.Val17631Ile)	rs749503285	0.00006
NM_001267550.2(TTN):c.53100T>G (p.Pro17700=)	rs373140387	0.00003
NM_001267550.2(TTN):c.53261T>C (p.Phe17754Ser)	rs749312983	0.00002
NM_001267550.2(TTN):c.53095C>T (p.Arg17699Cys)	rs760963888	0.00001

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