List of variants in gene CHEK2 reported as uncertain significance for Familial prostate cancer

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_007194.4(CHEK2):c.176C>A (p.Thr59Lys)	rs149991239	0.00002
NM_007194.4(CHEK2):c.383C>T (p.Pro128Leu)	rs587781879	0.00001
NM_007194.4(CHEK2):c.565A>G (p.Ile189Val)	rs587780185	0.00001
NM_007194.4(CHEK2):c.73G>A (p.Val25Ile)	rs142243299	0.00001
NM_007194.4(CHEK2):c.1055A>T (p.Asn352Ile)
NM_007194.4(CHEK2):c.1567del (p.Arg523fs)	rs587782684
NM_007194.4(CHEK2):c.288A>T (p.Leu96Phe)	rs767758092

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