List of variants in gene combination LOC130003020, NOTCH1 reported as benign for not provided

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_017617.5(NOTCH1):c.-152T>C	rs7028061	0.68312
NM_017617.5(NOTCH1):c.52G>A (p.Ala18Thr)	rs754613772	0.00015
NM_017617.5(NOTCH1):c.-215_-203del	rs532729798

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