List of variants in gene NPHP1 reported as likely pathogenic for cerebellar degeneration

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001128178.3(NPHP1):c.771+169G>T	rs150520157	0.00025
NM_001128178.3(NPHP1):c.1083+1G>A	rs564605452	0.00001
NM_001128178.3(NPHP1):c.144-1G>A	rs752708835	0.00001
NM_001128178.3(NPHP1):c.329+1G>A	rs376974221	0.00001
NC_000002.11:g.(?_110880912)_(110886837_110889255)del

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