List of variants in gene combination LOC111365204, PRDM13 reported as pathogenic for inherited retinal dystrophy

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NC_000006.12:g.99593111G>C	rs1554264613	0.00001
NC_000006.12:g.99593030G>T	rs1554264612
NC_000006.12:g.99593098A>C	rs1583607800
NC_000006.12:g.99593164C>T	rs1554264616

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