ClinVar Miner

List of variants in gene combination LOC126806429, TTN reported as uncertain significance by Biesecker Lab/Clinical Genomics Section, National Institutes of Health

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.19995A>T (p.Glu6665Asp)	rs146828735	0.00002
NM_001267550.2(TTN):c.20170G>T (p.Val6724Phe)	rs140143513

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