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

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

Total variants with conflicting interpretations: 14

HGVS	dbSNP	gnomAD frequency
NM_004415.4(DSP):c.726+219T>G	rs2076295	0.45371
NM_007294.4(BRCA1):c.*1287C>T	rs12516	0.30331
NM_001001331.4(ATP2B2):c.1437C>T (p.Asn479=)	rs2289274	0.27068
NM_000354.5(SERPINA7):c.909G>T (p.Leu303Phe)	rs1804495	0.12108
NM_019616.4(F7):c.1172G>A (p.Arg391Gln)	rs6046	0.11574
NM_001378454.1(ALMS1):c.671C>A (p.Pro224His)	rs11889925	0.01714
NM_022168.4(IFIH1):c.1641+1G>C	rs35337543	0.00707
NM_000545.8(HNF1A):c.1165T>G (p.Leu389Val)	rs115080759	0.00198
NM_001377265.1(MAPT):c.1630G>A (p.Ala544Thr)	rs143624519	0.00180
NM_014009.4(FOXP3):c.176C>G (p.Ser59Cys)	rs199917616	0.00139
NM_000017.4(ACADS):c.1108A>G (p.Met370Val)	rs566325901	0.00009
NM_000458.4(HNF1B):c.660T>C (p.Asp220=)	rs779375959	0.00007
NM_013254.4(TBK1):c.1839G>T (p.Leu613Phe)	rs368859659	0.00003
NM_003661.4(APOL1):c.1164_1169del (p.Asn388_Tyr389del)	rs71785313

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