List of variants in gene KIF2A 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: 28

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HGVS	dbSNP	gnomAD frequency
NM_001098511.3(KIF2A):c.562G>A (p.Val188Ile)	rs777382535	0.00002
NM_001098511.3(KIF2A):c.1024G>A (p.Ala342Thr)	rs758143705	0.00001
NM_001098511.3(KIF2A):c.1279T>C (p.Ser427Pro)	rs1554042228	0.00001
NM_001098511.3(KIF2A):c.1109A>G (p.Tyr370Cys)	rs2531354655
NM_001098511.3(KIF2A):c.1153A>G (p.Arg385Gly)
NM_001098511.3(KIF2A):c.1162G>C (p.Glu388Gln)
NM_001098511.3(KIF2A):c.1165G>C (p.Asp389His)	rs2531356625
NM_001098511.3(KIF2A):c.1409C>T (p.Ala470Val)	rs2111960708
NM_001098511.3(KIF2A):c.1479A>C (p.Arg493Ser)	rs2531361914
NM_001098511.3(KIF2A):c.1486G>A (p.Gly496Ser)	rs2111964836
NM_001098511.3(KIF2A):c.1534G>A (p.Val512Met)	rs2111964949
NM_001098511.3(KIF2A):c.1610G>A (p.Cys537Tyr)
NM_001098511.3(KIF2A):c.1624A>T (p.Asn542Tyr)	rs2531365123
NM_001098511.3(KIF2A):c.1750T>G (p.Ser584Ala)	rs2111983205
NM_001098511.3(KIF2A):c.1799A>G (p.Asp600Gly)	rs2111986043
NM_001098511.3(KIF2A):c.202C>T (p.Pro68Ser)
NM_001098511.3(KIF2A):c.2150-2A>C	rs2112019070
NM_001098511.3(KIF2A):c.320_321insGG (p.Arg108fs)
NM_001098511.3(KIF2A):c.328A>C (p.Asn110His)	rs2111915930
NM_001098511.3(KIF2A):c.355C>G (p.Arg119Gly)	rs1467202590
NM_001098511.3(KIF2A):c.385T>C (p.Ser129Pro)	rs2111924785
NM_001098511.3(KIF2A):c.461G>A (p.Arg154His)	rs1219221959
NM_001098511.3(KIF2A):c.593T>A (p.Met198Lys)	rs1748040065
NM_001098511.3(KIF2A):c.715C>T (p.Gln239Ter)	rs2531344461
NM_001098511.3(KIF2A):c.797C>T (p.Thr266Ile)
NM_001098511.3(KIF2A):c.850G>A (p.Ala284Thr)	rs2531344728
NM_001098511.3(KIF2A):c.869A>G (p.Tyr290Cys)
NM_001098511.3(KIF2A):c.956A>G (p.Lys319Arg)	rs2531351639

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