List of variants in gene LOC129999152, MDFIC studied for Inborn genetic diseases

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001166345.3(MDFIC):c.37G>T (p.Val13Leu)	rs1263865542	0.00001
NM_001166345.3(MDFIC):c.-45C>G
NM_001166345.3(MDFIC):c.-5G>A
NM_001166345.3(MDFIC):c.1A>C (p.Met1Leu)	rs1047880162
NM_001166345.3(MDFIC):c.2T>A (p.Met1Lys)	rs2485925715

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