List of variants in gene MMD reported as uncertain significance

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_012329.3(MMD):c.122C>T (p.Pro41Leu)	rs185564781	0.00008
NM_012329.3(MMD):c.12G>T (p.Lys4Asn)	rs1328402238	0.00001
NM_012329.3(MMD):c.58C>T (p.Arg20Cys)	rs746547063	0.00001
NM_012329.3(MMD):c.130G>C (p.Val44Leu)
NM_012329.3(MMD):c.190A>T (p.Ile64Phe)	rs2509255237
NM_012329.3(MMD):c.23A>G (p.Gln8Arg)
NM_012329.3(MMD):c.526G>A (p.Asp176Asn)
NM_012329.3(MMD):c.598A>G (p.Ile200Val)
NM_012329.3(MMD):c.9C>A (p.Phe3Leu)

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