List of variants in gene PRDM5 reported as likely benign for Brittle cornea syndrome 2

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_018699.4(PRDM5):c.1283-5C>T	rs185134294	0.00213
NM_018699.4(PRDM5):c.1282+9C>T	rs79915407	0.00011
NM_018699.4(PRDM5):c.300+17C>T	rs376707809	0.00008

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