List of variants in gene PROM1 reported as likely pathogenic by NIHR Bioresource Rare Diseases, University of Cambridge

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_006017.3(PROM1):c.1002+5G>A	rs1196489060	0.00001
NM_006017.3(PROM1):c.1117C>T (p.Arg373Cys)	rs137853006
NM_006017.3(PROM1):c.1177_1178del (p.Ile393fs)	rs746174328
NM_006017.3(PROM1):c.1710C>A (p.Tyr570Ter)	rs201644238

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