List of variants in gene KRT5 reported as 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000424.4(KRT5):c.555+9C>T	rs638907	0.18403
NM_000424.4(KRT5):c.1582A>G (p.Ser528Gly)	rs11549950	0.17563
NM_000424.4(KRT5):c.1065A>C (p.Thr355=)	rs4761924	0.15330
NM_000424.4(KRT5):c.1627G>A (p.Gly543Ser)	rs11549949	0.15185
NM_000424.4(KRT5):c.351C>T (p.Leu117=)	rs11549951	0.07903
NM_000424.4(KRT5):c.413G>A (p.Gly138Glu)	rs11170164	0.05271
NM_000424.4(KRT5):c.142A>C (p.Arg48=)	rs61747180	0.01877
NM_000424.4(KRT5):c.259T>G (p.Phe87Val)	rs61747188	0.01764
NM_000424.4(KRT5):c.156G>A (p.Ala52=)	rs74093478	0.01559
NM_000424.4(KRT5):c.1071C>T (p.Ala357=)	rs149467228	0.00503

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