List of variants in gene combination LOC112841608, SNRNP200 reported as uncertain significance for retinal disorder

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.-95G>A	rs780044707	0.00026
NM_014014.5(SNRNP200):c.-16C>T	rs375009722	0.00004
NM_014014.5(SNRNP200):c.-27G>A	rs886056469	0.00001

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