ClinVar Miner

List of variants in gene combination LOC126806429, TTN reported as uncertain significance by Clinical Genetics, Academic Medical Center

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.20057G>A (p.Arg6686Gln)	rs202022304	0.00004
NM_001267550.2(TTN):c.20138A>C (p.Lys6713Thr)	rs1410340266

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