List of variants in gene SNRNP200 reported as likely pathogenic by Institute of Human Genetics, Univ. Regensburg, Univ. Regensburg

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_014014.5(SNRNP200):c.1792C>T (p.Arg598Cys)	rs367922991	0.00010
NM_014014.5(SNRNP200):c.1996C>T (p.Arg666Cys)	rs200546584	0.00001
NM_014014.5(SNRNP200):c.2042G>A (p.Arg681His)	rs527236113

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