Variants with conflicting interpretations "likely risk allele" and "risk factor"

Submission 1 (likely risk allele) minimum review status:		Submission 1 (likely risk allele) method:
Submission 2 (risk factor) minimum review status:		Submission 2 (risk factor) method:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 5

HGVS	dbSNP	gnomAD frequency
NM_000636.4(SOD2):c.47T>C (p.Val16Ala)	rs4880	0.47242
NM_003661.4(APOL1):c.1024A>G (p.Ser342Gly)	rs73885319	0.06773
NM_001379610.1(SPINK1):c.101A>G (p.Asn34Ser)	rs17107315	0.00797
NM_003661.4(APOL1):c.1164_1169del (p.Asn388_Tyr389del)	rs71785313
NM_022162.3(NOD2):c.3019dup (p.Leu1007fs)	rs2066847

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