List of variants in gene MBD5 reported as uncertain significance by Mendelics

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_001378120.1(MBD5):c.1058C>G (p.Ser353Cys)	rs1448983984
NM_001378120.1(MBD5):c.114-3C>T	rs2105571139
NM_001378120.1(MBD5):c.1472G>C (p.Arg491Thr)	rs1024254683
NM_001378120.1(MBD5):c.2548A>G (p.Ile850Val)	rs1574476665
NM_001378120.1(MBD5):c.4540G>C (p.Glu1514Gln)	rs1296916399

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