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

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_002230.4(JUP):c.2207C>T (p.Pro736Leu)	rs151178348	0.00022
NM_002230.4(JUP):c.1172G>A (p.Ser391Asn)	rs199826380	0.00016
NM_002230.4(JUP):c.352G>A (p.Glu118Lys)	rs149004293	0.00011
NM_002230.4(JUP):c.1862T>C (p.Ile621Thr)	rs752594411	0.00009
NM_002230.4(JUP):c.1982G>A (p.Arg661Gln)	rs555499592	0.00008
NM_002230.4(JUP):c.427G>A (p.Ala143Thr)	rs375788626	0.00007
NM_002230.4(JUP):c.56C>T (p.Thr19Ile)	rs570878629	0.00007
NM_002230.4(JUP):c.568G>A (p.Val190Met)	rs370143312	0.00006

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