List of variants in gene combination LOC130059035, RPGRIP1L reported as uncertain significance 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
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_015272.5(RPGRIP1L):c.-9C>T	rs779839225	0.00143
NM_015272.5(RPGRIP1L):c.-16A>G	rs909461672
NM_015272.5(RPGRIP1L):c.-8G>T	rs1020579838

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