List of variants in gene CHEK2 reported as likely benign by University of Washington Department of Laboratory Medicine, University of Washington

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: 20

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HGVS	dbSNP	gnomAD frequency
NM_007194.4(CHEK2):c.1461+783C>T	rs114608104	0.01709
NM_007194.4(CHEK2):c.592+1802A>G	rs17885996	0.00506
NM_007194.4(CHEK2):c.792+128C>T	rs149538098	0.00204
NM_007194.4(CHEK2):c.1461+1775T>C	rs562452153	0.00195
NM_007194.4(CHEK2):c.1096-129A>T	rs574744424	0.00192
NM_007194.4(CHEK2):c.1375+140G>C	rs17886236	0.00190
NM_007194.4(CHEK2):c.847-1329T>C	rs188142621	0.00147
NM_007194.4(CHEK2):c.1375+121T>C	rs555987511	0.00137
NM_007194.4(CHEK2):c.320-5T>A	rs121908700	0.00070
NM_007194.4(CHEK2):c.1462-181A>T	rs869312552	0.00052
NM_007194.4(CHEK2):c.-6-3504A>G	rs192508267	0.00026
NM_007194.4(CHEK2):c.592+1705C>A	rs532061616	0.00026
NM_007194.4(CHEK2):c.909-74T>C	rs568812233	0.00020
NM_007194.4(CHEK2):c.909-61T>A	rs143467815	0.00011
NM_007194.4(CHEK2):c.846+664C>T	rs869312551	0.00010
NM_007194.4(CHEK2):c.1542+208C>T	rs200110854	0.00007
NM_007194.4(CHEK2):c.793-122G>A	rs869312548	0.00004
NM_007194.4(CHEK2):c.1009-166A>G	rs869312554	0.00002
NM_007194.4(CHEK2):c.793-107G>T	rs869312553
NM_007194.4(CHEK2):c.909-90C>T	rs869312549

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