List of variants in gene S100A13 reported as uncertain significance for not specified

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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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001024211.2(S100A13):c.221A>G (p.Asn74Ser)	rs200573399	0.00003
NM_001024211.2(S100A13):c.83G>A (p.Gly28Asp)	rs370377697	0.00002
NM_001024211.2(S100A13):c.198T>A (p.Asn66Lys)	rs367630492	0.00001
NM_001024211.2(S100A13):c.176A>G (p.Lys59Arg)
NM_001024211.2(S100A13):c.206C>T (p.Ser69Leu)	rs1283885643
NM_001024211.2(S100A13):c.20C>T (p.Thr7Ile)	rs2524524847
NM_001024211.2(S100A13):c.239T>C (p.Ile80Thr)
NM_001024211.2(S100A13):c.261C>G (p.Ile87Met)
NM_001024211.2(S100A13):c.284T>C (p.Ile95Thr)	rs2464300307
NM_001024211.2(S100A13):c.32A>G (p.Glu11Gly)
NM_001024211.2(S100A13):c.53C>T (p.Thr18Ile)	rs1667633997

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