Variants with conflicting interpretations "likely benign" from GeneKor MSA and "benign" from any submitter

Minimum review status of the submission from GeneKor MSA:		Collection method of the submission from GeneKor MSA:
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_139076.3(ABRAXAS1):c.1117G>A (p.Asp373Asn)	rs13125836	0.04289
NM_000535.7(PMS2):c.52A>G (p.Ile18Val)	rs63750123	0.00861
NM_000051.4(ATM):c.146C>G (p.Ser49Cys)	rs1800054	0.00712
NM_000057.4(BLM):c.4076+4T>G	rs183176301	0.00436
NM_005732.4(RAD50):c.980G>A (p.Arg327His)	rs28903091	0.00207
NM_058216.3(RAD51C):c.790G>A (p.Gly264Ser)	rs147241704	0.00207
NM_000179.3(MSH6):c.663A>C (p.Glu221Asp)	rs41557217	0.00064

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