Variants in gene PDZD7 with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) 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_001195263.2(PDZD7):c.1655dup (p.Ala553fs)	rs1378470761	0.00001
NM_001195263.2(PDZD7):c.682G>A (p.Gly228Arg)	rs753034799	0.00001
NM_001195263.2(PDZD7):c.1011C>G (p.Tyr337Ter)
NM_001195263.2(PDZD7):c.1500C>A (p.Tyr500Ter)	rs953422571
NM_001195263.2(PDZD7):c.2107del (p.Ser703fs)	rs397516633
NM_001195263.2(PDZD7):c.2692dup (p.Ala898fs)	rs1177831852
NM_001195263.2(PDZD7):c.307G>C (p.Gly103Arg)	rs148695069
NM_001195263.2(PDZD7):c.490C>T (p.Arg164Trp)	rs200664140
NM_001195263.2(PDZD7):c.854T>G (p.Met285Arg)	rs1554835827
NM_001195263.2(PDZD7):c.925C>T (p.Arg309Ter)
NM_001195263.2(PDZD7):c.993C>A (p.Cys331Ter)	rs1468599549

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