List of variants in gene MIPEP reported as likely pathogenic for not provided

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_005932.4(MIPEP):c.916C>T (p.Leu306Phe)	rs143912947	0.00002
NM_005932.4(MIPEP):c.358G>A (p.Asp120Asn)	rs780533096	0.00001
NM_005932.4(MIPEP):c.1848+2T>G

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