List of variants in gene NHS reported as uncertain significance for cataract

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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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001291867.2(NHS):c.1228C>G (p.Gln410Glu)	rs375878222	0.00012
NM_001291867.2(NHS):c.152C>T (p.Ala51Val)	rs727504039	0.00005
NM_001291867.2(NHS):c.546C>G (p.Asp182Glu)	rs759834255	0.00001
NM_001291867.2(NHS):c.176_177delinsAA (p.Arg59Gln)	rs797045739
NM_001291867.2(NHS):c.4783A>C (p.Thr1595Pro)	rs794727936
NM_001291867.2(NHS):c.566-52355A>G

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