List of variants in gene CHEK2 reported as uncertain significance for digestive system 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: 25

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HGVS	dbSNP	gnomAD frequency
NM_007194.4(CHEK2):c.470T>C (p.Ile157Thr)	rs17879961	0.00434
NM_007194.4(CHEK2):c.-6G>A	rs376995740	0.00065
NM_007194.4(CHEK2):c.1451C>T (p.Pro484Leu)	rs564605612	0.00036
NM_007194.4(CHEK2):c.1312G>T (p.Asp438Tyr)	rs200050883	0.00034
NM_007194.4(CHEK2):c.1427C>T (p.Thr476Met)	rs142763740	0.00032
NM_007194.4(CHEK2):c.715G>A (p.Glu239Lys)	rs121908702	0.00016
NM_007194.4(CHEK2):c.751A>T (p.Ile251Phe)	rs587780189	0.00009
NM_007194.4(CHEK2):c.1111C>T (p.His371Tyr)	rs531398630	0.00008
NM_007194.4(CHEK2):c.134C>T (p.Thr45Met)	rs558321010	0.00008
NM_007194.4(CHEK2):c.1582G>A (p.Glu528Lys)	rs138040612	0.00006
NM_007194.4(CHEK2):c.1423T>A (p.Phe475Ile)	rs370968992	0.00004
NM_007194.4(CHEK2):c.400G>C (p.Asp134His)	rs372874441	0.00004
NM_007194.4(CHEK2):c.962A>C (p.Glu321Ala)	rs374395284	0.00004
NM_007194.4(CHEK2):c.953G>A (p.Arg318His)	rs143611747	0.00003
NM_007194.4(CHEK2):c.931G>A (p.Asp311Asn)	rs587782347	0.00002
NM_007194.4(CHEK2):c.1096-6T>G	rs1180195480	0.00001
NM_007194.4(CHEK2):c.335A>G (p.Asn112Ser)	rs876660788	0.00001
NM_007194.4(CHEK2):c.434G>A (p.Arg145Gln)	rs587781667	0.00001
NM_007194.4(CHEK2):c.565A>G (p.Ile189Val)	rs587780185	0.00001
NM_007194.4(CHEK2):c.906A>C (p.Glu302Asp)	rs587780190	0.00001
NM_007194.4(CHEK2):c.319+3965C>T	rs766676371
NM_007194.4(CHEK2):c.686G>A (p.Gly229Asp)	rs778212685
NM_007194.4(CHEK2):c.749TCA[1] (p.Ile251del)	rs1601783129
NM_007194.4(CHEK2):c.796C>A (p.Pro266Thr)	rs1601777776
NM_007194.4(CHEK2):c.920G>A (p.Gly307Glu)	rs876661053

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