List of variants in gene combination LOC126859653, SKIC2 reported as uncertain significance for immune system disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_006929.5(SKIC2):c.1020T>C (p.Val340=)	rs61761944	0.00058
NM_006929.5(SKIC2):c.1120C>T (p.Arg374Ter)	rs200818962	0.00011
NM_006929.5(SKIC2):c.1132G>A (p.Gly378Arg)	rs776131482	0.00004
NM_006929.5(SKIC2):c.954C>T (p.Ala318=)	rs577271106	0.00004
NM_006929.5(SKIC2):c.990C>T (p.Val330=)	rs778024754	0.00004
NM_006929.5(SKIC2):c.1243C>T (p.Arg415Trp)	rs138507648	0.00003
NM_006929.5(SKIC2):c.1145T>A (p.Leu382Gln)	rs764335100	0.00002
NM_006929.5(SKIC2):c.1114G>A (p.Asp372Asn)
NM_006929.5(SKIC2):c.1151C>T (p.Thr384Ile)	rs886061307
NM_006929.5(SKIC2):c.1177G>A (p.Ala393Thr)	rs1772553546

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