Variants in gene ENPP1 with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_006208.3(ENPP1):c.-13G>A	rs535293574	0.01629
NM_006208.3(ENPP1):c.2757A>T (p.Pro919=)	rs73541508	0.00178
NM_006208.3(ENPP1):c.1056T>G (p.Ala352=)	rs150279426	0.00115
NM_006208.3(ENPP1):c.2336C>A (p.Thr779Asn)	rs200239821	0.00021
NM_006208.3(ENPP1):c.2462G>A (p.Arg821His)	rs367759638	0.00004
NM_006208.3(ENPP1):c.1791T>C (p.Asn597=)	rs548504035	0.00001
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[22]	rs59956343
NM_006208.3(ENPP1):c.523G>A (p.Asp175Asn)

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