List of variants in gene NRAP reported as uncertain significance 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_198060.4(NRAP):c.2963A>C (p.Gln988Pro)	rs150955833	0.00177
NM_198060.4(NRAP):c.4504C>T (p.Arg1502Ter)	rs201084642	0.00024
NM_198060.4(NRAP):c.2242G>A (p.Gly748Arg)	rs145550333	0.00003
NM_198060.4(NRAP):c.1810C>T (p.His604Tyr)	rs776270525
NM_198060.4(NRAP):c.2288C>A (p.Thr763Asn)	rs2493526759
NM_198060.4(NRAP):c.2419T>C (p.Phe807Leu)
NM_198060.4(NRAP):c.2788G>A (p.Val930Met)
NM_198060.4(NRAP):c.3186+3G>C	rs1847547807
NM_198060.4(NRAP):c.3260G>T (p.Ser1087Ile)
NM_198060.4(NRAP):c.4177G>A (p.Glu1393Lys)
NM_198060.4(NRAP):c.4618C>T (p.Arg1540Trp)
NM_198060.4(NRAP):c.5035C>T (p.Arg1679Trp)

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