List of variants in gene BRWD3 reported as uncertain significance for Non-syndromic X-linked intellectual disability

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_153252.5(BRWD3):c.*244CA[2]	rs1057516004
NM_153252.5(BRWD3):c.-229_-228dup	rs1057516006
NM_153252.5(BRWD3):c.-265TC[7]	rs1057516007
NM_153252.5(BRWD3):c.3326-14del	rs765175433
NM_153252.5(BRWD3):c.3326-26dup	rs765175433

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