List of variants in gene SKIC2 reported as benign by Illumina Laboratory Services, Illumina

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_006929.5(SKIC2):c.3201T>C (p.Tyr1067=)	rs410851	0.79487
NM_006929.5(SKIC2):c.640A>C (p.Met214Leu)	rs437179	0.77931
NM_006929.5(SKIC2):c.3212C>T (p.Ala1071Val)	rs449643	0.19166
NM_006929.5(SKIC2):c.452A>G (p.Gln151Arg)	rs438999	0.11787
NM_006929.5(SKIC2):c.2659G>A (p.Asp887Asn)	rs3911893	0.05545
NM_006929.5(SKIC2):c.2749G>A (p.Val917Met)	rs106287	0.02061
NM_006929.5(SKIC2):c.279C>G (p.Val93=)	rs11541400	0.00655
NM_006929.5(SKIC2):c.2574G>A (p.Val858=)	rs139281450	0.00314
NM_006929.5(SKIC2):c.2211G>A (p.Pro737=)	rs2280773	0.00296
NM_006929.5(SKIC2):c.384T>C (p.Ala128=)	rs3895064	0.00113
NM_006929.5(SKIC2):c.741C>G (p.Cys247Trp)	rs149410050	0.00112
NM_006929.5(SKIC2):c.23-14A>T	rs145129911	0.00109
NM_006929.5(SKIC2):c.*19T>C	rs2075702	0.00094
NM_006929.5(SKIC2):c.774A>G (p.Glu258=)	rs143738551	0.00045
NM_006929.5(SKIC2):c.3070-7T>C	rs201101301	0.00011
NM_006929.5(SKIC2):c.2052C>T (p.His684=)	rs61761946

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