List of variants in gene MNX1 reported as pathogenic by OMIM

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
MNX1, 24-BP DEL/2-BP INS, NT577
NM_005515.4(MNX1):c.340del (p.His114fs)
NM_005515.4(MNX1):c.53dup (p.Arg19fs)	rs1554594329
NM_005515.4(MNX1):c.570del (p.Gly191fs)
NM_005515.4(MNX1):c.736A>T (p.Thr246Ser)	rs121912548
NM_005515.4(MNX1):c.775C>T (p.Gln259Ter)	rs121912546
NM_005515.4(MNX1):c.844G>T (p.Glu282Ter)	rs121912549
NM_005515.4(MNX1):c.852+1G>A	rs1563700419
NM_005515.4(MNX1):c.853-2A>G	rs1563700090

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