ClinVar Miner

List of variants in gene combination LOC126806420, TTN reported as likely pathogenic by Revvity Omics, Revvity

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)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.100171+1G>A	rs1691855470
NM_001267550.2(TTN):c.100172-1G>A	rs2154137558

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