List of variants in gene NSDHL reported as benign by GeneDx

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_015922.3(NSDHL):c.132T>G (p.Gly44=)	rs5969919	0.83345
NM_015922.3(NSDHL):c.789+209C>T	rs2071255	0.16217
NM_015922.3(NSDHL):c.-43-242C>T	rs6627272	0.06379
NM_015922.3(NSDHL):c.109-262A>G	rs6526132	0.06155
NM_015922.3(NSDHL):c.414+184_414+187del	rs201312305	0.02579
NM_015922.3(NSDHL):c.544-197G>T	rs148372725	0.02288
NM_015922.3(NSDHL):c.942C>T (p.Ile314=)	rs35375481	0.00776
NM_015922.3(NSDHL):c.25A>G (p.Met9Val)	rs35529894	0.00457
NM_015922.3(NSDHL):c.1054C>T (p.Leu352=)	rs142351862	0.00444
NM_015922.3(NSDHL):c.268-319G>A	rs4828729
NM_015922.3(NSDHL):c.687-340A>G	rs2071254
NM_015922.3(NSDHL):c.789+235G>C	rs2071256

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