List of variants in gene SNRNP200 reported as benign for Retinitis pigmentosa

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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: 14

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HGVS	dbSNP	gnomAD frequency
NM_014014.5(SNRNP200):c.3550T>C (p.Leu1184=)	rs3171927	0.22368
NM_014014.5(SNRNP200):c.5386C>T (p.Leu1796=)	rs34435094	0.02646
NM_014014.5(SNRNP200):c.2422-8C>T	rs79583389	0.02643
NM_014014.5(SNRNP200):c.5775C>G (p.Ala1925=)	rs72825880	0.01765
NM_014014.5(SNRNP200):c.210-11A>T	rs113877776	0.00739
NM_014014.5(SNRNP200):c.5933G>C (p.Gly1978Ala)	rs75956769	0.00593
NM_014014.5(SNRNP200):c.3654C>T (p.Ser1218=)	rs3214060	0.00353
NM_014014.5(SNRNP200):c.4165G>A (p.Val1389Ile)	rs143898031	0.00328
NM_014014.5(SNRNP200):c.5418C>T (p.Asp1806=)	rs72937669	0.00267
NM_014014.5(SNRNP200):c.2800A>G (p.Thr934Ala)	rs149616320	0.00042
NM_014014.5(SNRNP200):c.*257C>G	rs560814451	0.00001
NM_014014.5(SNRNP200):c.5983G>A (p.Ala1995Thr)	rs201691299
NM_014014.5(SNRNP200):c.723G>A (p.Ser241=)	rs2276647
NM_014014.5(SNRNP200):c.732C>T (p.Leu244=)	rs199688602

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