Variants in gene ENPP1 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 18

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HGVS	dbSNP	gnomAD frequency
NM_006208.3(ENPP1):c.2320C>T (p.Arg774Cys)	rs28933977	0.02826
NM_006208.3(ENPP1):c.-10C>T	rs750410843	0.02463
NM_006208.3(ENPP1):c.1831C>G (p.Leu611Val)	rs79079368	0.01455
NM_006208.3(ENPP1):c.2106T>C (p.Ser702=)	rs7750837	0.01366
NM_006208.3(ENPP1):c.618-20T>G	rs143637835	0.00689
NM_006208.3(ENPP1):c.2124C>A (p.Phe708Leu)	rs140521704	0.00260
NM_006208.3(ENPP1):c.2757A>T (p.Pro919=)	rs73541508	0.00178
NM_006208.3(ENPP1):c.2101-10del	rs200562612	0.00116
NM_006208.3(ENPP1):c.522C>T (p.Gly174=)	rs144882196	0.00080
NM_006208.3(ENPP1):c.2336C>A (p.Thr779Asn)	rs200239821	0.00021
NM_006208.3(ENPP1):c.1540T>C (p.Leu514=)	rs536023117	0.00007
NM_006208.3(ENPP1):c.313+8_313+9dup	rs377330284
NM_006208.3(ENPP1):c.313+9GT[16]	rs59956343
NM_006208.3(ENPP1):c.313+9GT[17]	rs59956343
NM_006208.3(ENPP1):c.313+9GT[20]	rs59956343
NM_006208.3(ENPP1):c.313+9GT[21]	rs59956343
NM_006208.3(ENPP1):c.313+9GT[22]	rs59956343
NM_006208.3(ENPP1):c.313+9del	rs377330284

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