List of variants in gene NDP 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: 6

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HGVS	dbSNP	gnomAD frequency
GRCh37/hg19 Xp11.3(chrX:43752453-43834126)x2
NM_000266.4(NDP):c.193_194insTTTTC	rs2147204553
NM_000266.4(NDP):c.-207-5T>C	rs2519320914
NM_000266.4(NDP):c.164G>C (p.Cys55Ser)	rs2519320442
NM_000266.4(NDP):c.174G>T (p.Lys58Asn)	rs2147209153
NM_000266.4(NDP):c.269G>C (p.Arg90Pro)	rs104894867

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