ClinVar Miner

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:
Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP
NM_007194.4(CHEK2):c.-6-3504A>G rs192508267
NM_007194.4(CHEK2):c.-7+136T>C rs869312550
NM_007194.4(CHEK2):c.1009-166A>G rs869312554
NM_007194.4(CHEK2):c.1096-129A>T rs574744424
NM_007194.4(CHEK2):c.1375+121T>C rs555987511
NM_007194.4(CHEK2):c.1375+140G>C rs17886236
NM_007194.4(CHEK2):c.1461+1775T>C rs562452153
NM_007194.4(CHEK2):c.1461+783C>T rs114608104
NM_007194.4(CHEK2):c.1462-181A>T rs869312552
NM_007194.4(CHEK2):c.1542+208C>T rs200110854
NM_007194.4(CHEK2):c.320-5T>A rs121908700
NM_007194.4(CHEK2):c.592+1705C>A rs532061616
NM_007194.4(CHEK2):c.592+1802A>G rs17885996
NM_007194.4(CHEK2):c.792+128C>T rs149538098
NM_007194.4(CHEK2):c.793-107G>T rs869312553
NM_007194.4(CHEK2):c.793-122G>A rs869312548
NM_007194.4(CHEK2):c.846+664C>T rs869312551
NM_007194.4(CHEK2):c.847-1329T>C rs188142621
NM_007194.4(CHEK2):c.909-61T>A rs143467815
NM_007194.4(CHEK2):c.909-74T>C rs568812233
NM_007194.4(CHEK2):c.909-90C>T rs869312549

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