List of variants in gene PROM1 reported as benign for Retinal macular dystrophy type 2

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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: 16

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HGVS	dbSNP	gnomAD frequency
NM_006017.3(PROM1):c.*1078A>G	rs3130	0.53265
NM_006017.3(PROM1):c.303+6G>A	rs2078622	0.39397
NM_006017.3(PROM1):c.2374-6T>C	rs6449209	0.34571
NM_006017.3(PROM1):c.2582+43C>T	rs11725522	0.22440
NM_006017.3(PROM1):c.*667A>C	rs2240688	0.21643
NM_006017.3(PROM1):c.2281-6C>G	rs3815344	0.20394
NM_006017.3(PROM1):c.1003-35A>C	rs2286458	0.09908
NM_006017.3(PROM1):c.786G>A (p.Ala262=)	rs2286455	0.09727
NM_006017.3(PROM1):c.129C>T (p.Thr43=)	rs10033086	0.09038
NM_006017.3(PROM1):c.15C>T (p.Leu5=)	rs10033189	0.06194
NM_006017.3(PROM1):c.1983+14G>A	rs4698436	0.04259
NM_006017.3(PROM1):c.228G>A (p.Leu76=)	rs76963591	0.03578
NM_006017.3(PROM1):c.1768-5C>T	rs55708318	0.03551
NM_006017.3(PROM1):c.631-14T>C	rs16892824	0.01810
NM_006017.3(PROM1):c.55T>G (p.Ser19Ala)	rs189108830	0.00928
NM_006017.3(PROM1):c.1345G>A (p.Val449Met)	rs200620291	0.00152

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