List of variants in gene FNDC3A reported as benign

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001079673.2(FNDC3A):c.3049A>G (p.Thr1017Ala)	rs45604939	0.04691
NM_001079673.2(FNDC3A):c.3132A>G (p.Lys1044=)	rs9316430	0.04590
NM_001079673.2(FNDC3A):c.319A>G (p.Ser107Gly)	rs34539036	0.02021
NM_001079673.2(FNDC3A):c.825C>T (p.Ser275=)	rs74965684	0.01021
NM_001079673.2(FNDC3A):c.1752C>T (p.Thr584=)	rs112538251	0.00663

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