Variants with conflicting interpretations "uncertain significance" from HLA Laboratory, Instituto Nacional de Enfermedades Respiratorias Ismael Cosio Villegas and "benign" from any submitter

Minimum review status of the submission from HLA Laboratory, Instituto Nacional de Enfermedades Respiratorias Ismael Cosio Villegas:		Collection method of the submission from HLA Laboratory, Instituto Nacional de Enfermedades Respiratorias Ismael Cosio Villegas:
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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 9

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HGVS	dbSNP	gnomAD frequency
NM_001065.4(TNFRSF1A):c.36A>G (p.Pro12=)	rs767455	0.39963
NM_001065.4(TNFRSF1A):c.625+10A>G	rs1800693	0.38055
NM_005656.4(TMPRSS2):c.478G>A (p.Val160Met)	rs12329760	0.25326
NM_001001331.4(ATP2B2):c.1551C>T (p.Gly517=)	rs2289273	0.10735
NM_001289125.3(IFNAR2):c.23T>C (p.Phe8Ser)	rs2229207	0.08893
NM_000602.5(SERPINE1):c.43G>A (p.Ala15Thr)	rs6092	0.07905
NM_138554.5(TLR4):c.896A>G (p.Asp299Gly)	rs4986790	0.06665
NC_000011.10:g.1219991G>T	rs35705950
NM_001289125.3(IFNAR2):c.541-50A>G

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