List of variants in gene combination LOC129992137, MSX1 reported as likely benign for tooth and nail syndrome

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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_002448.3(MSX1):c.218C>T (p.Pro73Leu)	rs201156596	0.00425
NM_002448.3(MSX1):c.95C>T (p.Ala32Val)	rs771408025	0.00041
NM_002448.3(MSX1):c.324G>T (p.Ala108=)	rs574606351	0.00022
NM_002448.3(MSX1):c.65G>A (p.Gly22Asp)	rs755151662	0.00011
NM_002448.3(MSX1):c.195G>A (p.Ala65=)	rs771658240	0.00007
NM_002448.3(MSX1):c.108C>A (p.Ala36=)	rs547137864	0.00004
NM_002448.3(MSX1):c.123C>A (p.Ala41=)	rs1001828551	0.00001
NM_002448.3(MSX1):c.89G>A (p.Gly30Asp)	rs1414674827	0.00001
NM_002448.3(MSX1):c.77G>C (p.Gly26Ala)	rs567549350

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