Variants with conflicting interpretations "likely pathogenic" from HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology and "pathogenic" from Women's Health and Genetics/Laboratory Corporation of America, LabCorp

Minimum review status of the submission from HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology:		Collection method of the submission from HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology:
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Show significances as they were submitted (without aggregation into standard terms)
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Total variants with conflicting interpretations: 10

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HGVS	dbSNP	gnomAD frequency
NM_001048174.2(MUTYH):c.452A>G (p.Tyr151Cys)	rs34612342	0.00168
NM_001354604.2(MITF):c.1273G>A (p.Glu425Lys)	rs149617956	0.00160
NM_000053.4(ATP7B):c.2605G>A (p.Gly869Arg)	rs191312027	0.00101
NM_000441.2(SLC26A4):c.1003T>C (p.Phe335Leu)	rs111033212	0.00077
NM_019109.5(ALG1):c.773C>T (p.Ser258Leu)	rs28939378	0.00036
NM_000303.3(PMM2):c.368G>A (p.Arg123Gln)	rs141498002	0.00017
NM_000527.5(LDLR):c.1747C>T (p.His583Tyr)	rs730882109	0.00003
NM_000370.3(TTPA):c.552G>A (p.Thr184=)	rs181109321	0.00002
NM_005061.3(RPL3L):c.80G>A (p.Gly27Asp)	rs770344400	0.00001
NM_000492.4(CFTR):c.350G>A (p.Arg117His)	rs78655421

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