List of variants in gene combination LOC129935185, TTN reported as uncertain significance for autosomal recessive limb-girdle muscular dystrophy type 2J

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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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.105134A>T (p.Asp35045Val)	rs1001393566	0.00001
NM_001267550.2(TTN):c.105149G>C (p.Arg35050Thr)	rs376175862	0.00001
NM_001267550.2(TTN):c.105133G>C (p.Asp35045His)
NM_001267550.2(TTN):c.105138_105164del (p.Glu35047_Glu35055del)
NM_001267550.2(TTN):c.105142G>A (p.Val35048Ile)	rs1689087953
NM_001267550.2(TTN):c.105145C>A (p.Pro35049Thr)	rs2154133549
NM_001267550.2(TTN):c.105151T>G (p.Ser35051Ala)
NM_001267550.2(TTN):c.105152C>T (p.Ser35051Phe)
NM_001267550.2(TTN):c.105154G>C (p.Val35052Leu)	rs751583336
NM_001267550.2(TTN):c.105166C>G (p.Leu35056Val)
NM_001267550.2(TTN):c.105174A>T (p.Arg35058Ser)
NM_001267550.2(TTN):c.105180G>T (p.Glu35060Asp)	rs56308529
NM_001267550.2(TTN):c.105180_105181delinsCA (p.Glu35060_Ala35061delinsAspThr)	rs1689075044

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