List of variants in gene NSDHL reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_015922.3(NSDHL):c.914T>G (p.Leu305Arg)	rs781948041	0.00001
NM_015922.3(NSDHL):c.1108C>T (p.Arg370Trp)	rs151248633
NM_015922.3(NSDHL):c.816C>A (p.Pro272=)	rs1328593149
NM_015922.3(NSDHL):c.842G>A (p.Arg281His)	rs782143078

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