Variants with conflicting interpretations "pathogenic" from Eurofins NTD LLC (GA) and "likely pathogenic" from Illumina Laboratory Services, Illumina

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_213599.3(ANO5):c.2498T>A (p.Met833Lys)	rs142073798	0.00014
NM_000232.5(SGCB):c.31C>T (p.Gln11Ter)	rs752492870	0.00007
NM_024809.5(TCTN2):c.1506-2A>G	rs374349989	0.00002
NM_000518.4(HBB):c.364G>C (p.Glu122Gln)	rs33946267
NM_013296.5(GPSM2):c.742del (p.Gly249fs)	rs528069912
Single allele

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