List of variants in gene SCNN1G reported as benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001039.4(SCNN1G):c.1176+14A>G	rs5740	0.75623
NM_001039.4(SCNN1G):c.474T>C (p.Ile158=)	rs5735	0.27157
NM_001039.4(SCNN1G):c.387T>C (p.Tyr129=)	rs5734	0.27146
NM_001039.4(SCNN1G):c.1947C>G (p.Leu649=)	rs5723	0.21902
NM_001039.4(SCNN1G):c.1432-7G>A	rs13306653	0.21894
NM_001039.4(SCNN1G):c.549C>T (p.Gly183=)	rs5737	0.06659
NM_001039.4(SCNN1G):c.547G>A (p.Gly183Ser)	rs5736	0.01206
NM_001039.4(SCNN1G):c.589G>A (p.Glu197Lys)	rs5738	0.00548

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