List of variants in gene CACNA1F reported as benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 27

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HGVS	dbSNP	gnomAD frequency
NC_000023.11:g.49233563=	rs5906758	0.99896
NM_001256789.3(CACNA1F):c.4100+131G>C	rs12009701	0.09780
NM_001256789.3(CACNA1F):c.1651+241A>G	rs58793970	0.09695
NM_001256789.3(CACNA1F):c.818-302C>G	rs7050910	0.09583
NM_001256789.3(CACNA1F):c.26-173C>G	rs7066652	0.09508
NM_001256789.3(CACNA1F):c.2335-89C>T	rs5906756	0.07887
NM_001256789.3(CACNA1F):c.5756G>A (p.Arg1919His)	rs33910054	0.06102
NM_001256789.3(CACNA1F):c.3236+55T>C	rs7066236	0.05349
NM_001256789.3(CACNA1F):c.2929-172C>T	rs111247255	0.05297
NM_001256789.3(CACNA1F):c.521+39C>T	rs112130833	0.05292
NM_001256789.3(CACNA1F):c.41C>T (p.Pro14Leu)	rs6520408	0.05244
NM_001256789.3(CACNA1F):c.26-182A>G	rs11796927	0.05142
NM_001256789.3(CACNA1F):c.5670+69C>T	rs61653156	0.04931
NM_001256789.3(CACNA1F):c.3597+44T>G	rs7886686	0.04281
NM_001256789.3(CACNA1F):c.3237-71G>C	rs73498062	0.04138
NM_001256789.3(CACNA1F):c.2673+3G>A	rs41312124	0.04106
NM_001256789.3(CACNA1F):c.2335-138G>A	rs56114689	0.03905
NM_001256789.3(CACNA1F):c.3597+131T>C	rs147150039	0.02827
NM_001256789.3(CACNA1F):c.1118+6=
NM_001256789.3(CACNA1F):c.1809= (p.Gly603=)
NM_001256789.3(CACNA1F):c.2289-202=	rs2904024
NM_001256789.3(CACNA1F):c.2387-19del	rs375791434
NM_001256789.3(CACNA1F):c.2391GGA[8] (p.Glu814dup)	rs112450928
NM_001256789.3(CACNA1F):c.3089+149dup	rs11403487
NM_001256789.3(CACNA1F):c.3237-16C>G	rs190434065
NM_001256789.3(CACNA1F):c.3276= (p.His1092=)
NM_001256789.3(CACNA1F):c.3597+212dup	rs139742315

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