List of variants in gene SNRNP200 reported as likely benign for Retinitis pigmentosa 33

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_014014.5(SNRNP200):c.5775C>G (p.Ala1925=)	rs72825880	0.01765
NM_014014.5(SNRNP200):c.3654C>T (p.Ser1218=)	rs3214060	0.00353
NM_014014.5(SNRNP200):c.5766C>T (p.Leu1922=)	rs147427344	0.00133
NM_014014.5(SNRNP200):c.2800A>G (p.Thr934Ala)	rs149616320	0.00042
NM_014014.5(SNRNP200):c.982+10T>C	rs371450437	0.00040
NM_014014.5(SNRNP200):c.4377C>T (p.Ile1459=)	rs191438128	0.00004
NM_014014.5(SNRNP200):c.382-13T>C	rs759075763
NM_014014.5(SNRNP200):c.5983G>A (p.Ala1995Thr)	rs201691299

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