List of variants in gene MNX1 reported as likely benign for bone disorder

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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: 11

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HGVS	dbSNP	gnomAD frequency
NM_005515.4(MNX1):c.372T>C (p.Ala124=)	rs867470183	0.00325
NM_005515.4(MNX1):c.691+10C>G	rs201139239	0.00022
NM_005515.4(MNX1):c.528G>A (p.Ala176=)	rs752182988	0.00017
NM_005515.4(MNX1):c.126A>G (p.Gly42=)	rs536068265	0.00016
NM_005515.4(MNX1):c.164G>C (p.Ser55Thr)	rs866277517	0.00006
NM_005515.4(MNX1):c.1193C>T (p.Pro398Leu)	rs548959409	0.00005
NM_005515.4(MNX1):c.853-4G>T	rs751247773	0.00005
NM_005515.4(MNX1):c.1059C>A (p.Asp353Glu)	rs756772840	0.00002
NM_005515.4(MNX1):c.692-18C>T	rs775967115	0.00001
NM_005515.4(MNX1):c.298GGC[5] (p.Gly105del)	rs757330807
NM_005515.4(MNX1):c.950_973del (p.Gly317_Gly324del)

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