List of variants in gene MKKS reported as likely benign by Fulgent Genetics, Fulgent Genetics

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_170784.3(MKKS):c.15A>G (p.Glu5=)	rs145396188	0.00074
NM_170784.3(MKKS):c.231G>A (p.Leu77=)	rs373913834	0.00035
NM_170784.3(MKKS):c.416G>A (p.Arg139Gln)	rs145045986	0.00031
NM_170784.3(MKKS):c.1356T>C (p.Ser452=)	rs201977053	0.00008
NM_170784.3(MKKS):c.822C>T (p.Asp274=)	rs761342904	0.00003
NM_170784.3(MKKS):c.1360C>T (p.Leu454=)	rs1210784201	0.00001
NM_170784.3(MKKS):c.1695T>C (p.Val565=)	rs554395344	0.00001
NM_170784.3(MKKS):c.210A>C (p.Thr70=)	rs1471154105	0.00001
NM_170784.3(MKKS):c.1162-12del	rs781066396
NM_170784.3(MKKS):c.207C>T (p.Val69=)	rs1382659817
NM_170784.3(MKKS):c.717C>T (p.Leu239=)	rs1214711344

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