List of variants in gene NLRP1 reported as likely benign for corneal disorder

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_033004.4(NLRP1):c.316G>A (p.Gly106Arg)	rs72827640	0.00324
NM_033004.4(NLRP1):c.923G>A (p.Arg308Gln)	rs140628502	0.00122
NM_033004.4(NLRP1):c.272-7C>G	rs202080927	0.00036
NM_033004.4(NLRP1):c.3228C>T (p.Asp1076=)	rs139890811	0.00004

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