List of variants in gene combination LOC126806423, TTN reported as uncertain significance for TTN-related disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.67706G>A (p.Arg22569Gln)	rs185620750	0.00031
NM_001267550.2(TTN):c.67604G>A (p.Ser22535Asn)	rs375676529	0.00012
NM_001267550.2(TTN):c.68097G>C (p.Gln22699His)	rs727504520	0.00008
NM_001267550.2(TTN):c.68083G>A (p.Ala22695Thr)	rs767279296	0.00001
NM_001267550.2(TTN):c.67781A>T (p.Asp22594Val)
NM_001267550.2(TTN):c.68092G>T (p.Val22698Phe)
NM_001267550.2(TTN):c.68189T>C (p.Leu22730Pro)
NM_001267550.2(TTN):c.68323A>G (p.Ile22775Val)

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