List of variants in gene MKKS reported as uncertain significance by GeneDx

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: 17

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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.1363G>A (p.Glu455Lys)	rs149626732	0.00019
NM_170784.3(MKKS):c.697A>C (p.Ile233Leu)	rs141201812	0.00016
NM_170784.3(MKKS):c.1625T>G (p.Leu542Trp)	rs372944937	0.00015
NM_170784.3(MKKS):c.757T>C (p.Ser253Pro)	rs201785599	0.00012
NM_170784.3(MKKS):c.1457G>A (p.Cys486Tyr)	rs375952682	0.00011
NM_170784.3(MKKS):c.463C>T (p.Arg155Cys)	rs755050269	0.00005
NM_170784.3(MKKS):c.7C>T (p.Arg3Cys)	rs779042065	0.00005
NM_170784.3(MKKS):c.1318C>G (p.Gln440Glu)	rs772537800	0.00002
NM_170784.3(MKKS):c.659T>C (p.Ile220Thr)	rs752587935	0.00002
NM_170784.3(MKKS):c.1259A>G (p.Tyr420Cys)	rs748071139	0.00001
NM_170784.3(MKKS):c.748G>A (p.Gly250Arg)	rs768929313	0.00001
NM_170784.3(MKKS):c.1307A>G (p.Asp436Gly)	rs746696111
NM_170784.3(MKKS):c.1313G>A (p.Cys438Tyr)	rs758821712
NM_170784.3(MKKS):c.1328T>C (p.Leu443Pro)	rs2514487025
NM_170784.3(MKKS):c.26C>T (p.Pro9Leu)	rs751314471
NM_170784.3(MKKS):c.8G>T (p.Arg3Leu)

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