List of variants in gene combination LOC126860794, NOTCH1 reported as likely 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: 15

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HGVS	dbSNP	gnomAD frequency
NM_017617.5(NOTCH1):c.6180+126G>A	rs79872302	0.00985
NM_017617.5(NOTCH1):c.6180+151C>T	rs75949473	0.00586
NM_017617.5(NOTCH1):c.5988G>A (p.Thr1996=)	rs186453356	0.00236
NM_017617.5(NOTCH1):c.6105C>T (p.Ala2035=)	rs188357478	0.00108
NM_017617.5(NOTCH1):c.5967T>C (p.Asp1989=)	rs73668311	0.00061
NM_017617.5(NOTCH1):c.6108C>T (p.Ala2036=)	rs369167693	0.00046
NM_017617.5(NOTCH1):c.6057C>T (p.Ala2019=)	rs758702512	0.00010
NM_017617.5(NOTCH1):c.6083-5C>T	rs199786076	0.00009
NM_017617.5(NOTCH1):c.6120T>C (p.Asn2040=)	rs201625763	0.00009
NM_017617.5(NOTCH1):c.6083-4G>A	rs570242146	0.00008
NM_017617.5(NOTCH1):c.6090C>T (p.Ser2030=)	rs773621396	0.00005
NM_017617.5(NOTCH1):c.6150C>T (p.Asn2050=)	rs757372588	0.00004
NM_017617.5(NOTCH1):c.5935-11C>T	rs768074148	0.00002
NM_017617.5(NOTCH1):c.6069C>T (p.Ala2023=)	rs375920679	0.00002
NM_017617.5(NOTCH1):c.6083-10T>G	rs1380449680	0.00002

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