List of variants in gene CHEK2 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 23

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HGVS	dbSNP	gnomAD frequency
NM_007194.4(CHEK2):c.1343T>G (p.Ile448Ser)	rs17886163	0.00555
NM_007194.4(CHEK2):c.592+50A>T	rs17881298	0.00270
NM_007194.4(CHEK2):c.684-432G>A	rs17879919	0.00232
NM_007194.4(CHEK2):c.254C>T (p.Pro85Leu)	rs17883862	0.00201
NM_007194.4(CHEK2):c.320-5T>A	rs121908700	0.00070
NM_007194.4(CHEK2):c.*18C>T	rs17884403	0.00037
NM_007194.4(CHEK2):c.1312G>T (p.Asp438Tyr)	rs200050883	0.00034
NM_007194.4(CHEK2):c.1497G>C (p.Leu499=)	rs587780890	0.00032
NM_007194.4(CHEK2):c.410G>A (p.Arg137Gln)	rs368570187	0.00012
NM_007194.4(CHEK2):c.556A>C (p.Asn186His)	rs146198085	0.00009
NM_007194.4(CHEK2):c.1111C>T (p.His371Tyr)	rs531398630	0.00008
NM_007194.4(CHEK2):c.1556G>T (p.Arg519Leu)	rs587780180	0.00006
NM_007194.4(CHEK2):c.542G>A (p.Arg181His)	rs121908701	0.00006
NM_007194.4(CHEK2):c.1008+8A>G	rs139986197	0.00004
NM_007194.4(CHEK2):c.1423T>A (p.Phe475Ile)	rs370968992	0.00004
NM_007194.4(CHEK2):c.1287G>A (p.Glu429=)	rs758102180	0.00001
NM_007194.4(CHEK2):c.132C>T (p.Ser44=)	rs199715101	0.00001
NM_007194.4(CHEK2):c.1566C>T (p.Pro522=)	rs202104749	0.00001
NM_007194.4(CHEK2):c.528G>C (p.Gly176=)	rs587780889	0.00001
NM_007194.4(CHEK2):c.661A>G (p.Ile221Val)	rs199749372	0.00001
NM_007194.4(CHEK2):c.714C>T (p.Phe238=)	rs864622322	0.00001
NM_007194.4(CHEK2):c.-6-3287A>C
NM_007194.4(CHEK2):c.593-11_593-7del	rs863224414

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