List of variants in gene combination DSG2, LOC130062340 reported as likely pathogenic for Arrhythmogenic right ventricular dysplasia 10

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001943.5(DSG2):c.3G>A (p.Met1Ile)	rs1021457619	0.00001
NM_001943.5(DSG2):c.45+1G>A	rs1568098570
NM_001943.5(DSG2):c.45+1G>C	rs1568098570
NM_001943.5(DSG2):c.45+1G>T	rs1568098570
NM_001943.5(DSG2):c.45+2T>C

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