Variants with conflicting interpretations "pathogenic" from Mayo Clinic Laboratories, Mayo Clinic and "risk factor" from any submitter

Minimum review status of the submission from Mayo Clinic Laboratories, Mayo Clinic:		Collection method of the submission from Mayo Clinic Laboratories, Mayo Clinic:
Minimum review status of the other submission:		Collection method of the other submission:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 7

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HGVS	dbSNP	gnomAD frequency
NM_000157.4(GBA1):c.1226A>G (p.Asn409Ser)	rs76763715	0.00191
NM_000186.4(CFH):c.3628C>T (p.Arg1210Cys)	rs121913059	0.00019
NM_000051.4(ATM):c.7271T>G (p.Val2424Gly)	rs28904921	0.00006
NM_000157.4(GBA1):c.1448T>C (p.Leu483Pro)	rs421016
NM_000186.4(CFH):c.3572C>T (p.Ser1191Leu)	rs460897
NM_002485.5(NBN):c.657_661del (p.Lys219fs)	rs587776650
NM_007294.4(BRCA1):c.5266dup (p.Gln1756fs)	rs80357906

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