List of variants in gene SKIC2 reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_006929.5(SKIC2):c.1705G>A (p.Val569Met)	rs144147284	0.00185
NM_006929.5(SKIC2):c.1654G>A (p.Gly552Arg)	rs144670908	0.00142
NM_006929.5(SKIC2):c.2752G>A (p.Val918Ile)	rs148798682	0.00024
NM_006929.5(SKIC2):c.585C>T (p.Asp195=)	rs145042380	0.00014
NM_006929.5(SKIC2):c.1368C>T (p.Thr456=)	rs139188277	0.00013
NM_006929.5(SKIC2):c.3070-7T>C	rs201101301	0.00011
NM_006929.5(SKIC2):c.300C>T (p.Ser100=)	rs766457865	0.00004
NM_006929.5(SKIC2):c.3672C>T (p.Ala1224=)	rs769349127	0.00003
NM_006929.5(SKIC2):c.3720G>A (p.Ala1240=)	rs761696355	0.00003
NM_006929.5(SKIC2):c.1704C>T (p.Pro568=)	rs770385536	0.00001
NM_006929.5(SKIC2):c.2442G>C (p.Trp814Cys)	rs148221996
NM_006929.5(SKIC2):c.2479-7T>C	rs190972540
NM_006929.5(SKIC2):c.3400-10T>C	rs776082934

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