List of variants in gene combination LOC126806430, TTN reported as benign 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.18903C>T (p.Thr6301=)	rs72648950	0.01956
NM_001267550.2(TTN):c.18390A>T (p.Thr6130=)	rs66523653	0.01518
NM_001267550.2(TTN):c.18531G>C (p.Val6177=)	rs370684491	0.00088
NM_001267550.2(TTN):c.18942C>T (p.Thr6314=)	rs572285982	0.00004
NM_001267550.2(TTN):c.18363G>A (p.Gln6121=)	rs375032616	0.00003
NM_001267550.2(TTN):c.18456T>C (p.His6152=)	rs756540833	0.00001

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