Variants with conflicting interpretations "likely pathogenic" from Eurofins Ntd Llc (ga) and "other" from any submitter

Minimum review status of the submission from Eurofins Ntd Llc (ga):		Collection method of the submission from Eurofins Ntd Llc (ga):
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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001127701.1(SERPINA1):c.187C>T (p.Arg63Cys)	rs28931570	0.00137
NM_000518.4(HBB):c.208G>A (p.Gly70Ser)	rs33947415	0.00064
NM_000295.5(SERPINA1):c.646+1G>T	rs751235320	0.00001
NM_000194.2(HPRT1):c.211G>C (p.Gly71Arg)	rs137852488
Single allele

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