List of variants in gene combination LOC112533672, UNC13D reported as benign for immune system disorder

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_199242.3(UNC13D):c.2830+37C>G	rs2290769	0.19638
NM_199242.3(UNC13D):c.2943G>A (p.Glu981=)	rs35628234	0.07237
NM_199242.3(UNC13D):c.2782C>T (p.Arg928Cys)	rs35037984	0.01713
NM_199242.3(UNC13D):c.2831-20A>T	rs149809768	0.00199
NM_199242.3(UNC13D):c.2710-8C>G	rs545824447	0.00057
NM_199242.3(UNC13D):c.2709+6G>T	rs199529082	0.00014
NM_199242.3(UNC13D):c.2896C>T (p.Arg966Trp)	rs118049905

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