List of variants in gene LOC129937587, NPHP3, NPHP3-ACAD11 studied for Meckel syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_153240.4(NPHP3):c.-69A>G	rs13099099	0.49619
NM_153240.4(NPHP3):c.-70C>T	rs886058006	0.00056

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