List of variants in gene UNC13D reported as uncertain significance by 3billion

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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_199242.3(UNC13D):c.3229_3235del (p.Arg1077fs)	rs766652119	0.00002
NM_199242.3(UNC13D):c.1055+5G>A
NM_199242.3(UNC13D):c.1193C>T (p.Ser398Leu)	rs747756030
NM_199242.3(UNC13D):c.3049G>A (p.Glu1017Lys)	rs776737156
NM_199242.3(UNC13D):c.902A>G (p.His301Arg)	rs2143891961

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