ClinVar Miner

List of variants reported as benign for Hereditary cancer-predisposing syndrome by GeneDx

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ClinVar version:
Total variants: 45
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HGVS dbSNP gnomAD frequency
NM_000051.4(ATM):c.2921+19dup rs56112367 0.00245
NM_000455.5(STK11):c.597+14del rs536282050 0.00067
NM_000179.3(MSH6):c.3438+11_3438+14del rs377746844 0.00023
NM_000179.3(MSH6):c.4001+11_4001+15dup rs587779302 0.00019
NM_000051.4(ATM):c.5005+7_5005+8del rs587780626 0.00009
NM_004360.5(CDH1):c.48+15_48+16del rs730881655 0.00006
NM_000455.5(STK11):c.*22dup rs730881967 0.00003
NM_000038.5:c.423-17insT
NM_000038.6(APC):c.423-4del rs730881230
NM_000051.4(ATM):c.2251-18dup rs730881284
NM_000051.4(ATM):c.2839-18dup rs730881287
NM_000051.4(ATM):c.3403-13dup rs3218681
NM_000051.4(ATM):c.3577-12del rs730881288
NM_000051.4(ATM):c.4437-14dup rs730881290
NM_000051.4(ATM):c.7927+13dup rs587781324
NM_000179.2:c.3557-4insT
NM_000179.3(MSH6):c.4001+2TAAC[2] rs267608132
NM_000179.3(MSH6):c.4001+4_4001+8dup rs587782853
NM_000249.3:c.1039-6insA
NM_000249.4(MLH1):c.1039-8_1039-7insTA rs535965616
NM_000251.3(MSH2):c.2210+11_2210+22del rs730881782
NM_000251.3(MSH2):c.942+17_942+29del rs11309117
NM_000314.8(PTEN):c.*10del rs756681683
NM_000314.8(PTEN):c.-663_-652del rs786204880
NM_000314.8(PTEN):c.165-24TTTG[2] rs786204877
NM_000314.8(PTEN):c.802-18_802-14del rs786204879
NM_000455.5(STK11):c.464+20del rs730881960
NM_000465.2:c.365-8insT
NM_000465.4(BARD1):c.216-14del rs56130510
NM_000546.6(TP53):c.96+15_96+30del rs730882010
NM_000546.6(TP53):c.96+15_96+31del rs730882011
NM_000546.6(TP53):c.96+41_97-54del rs59758982
NM_000546.6(TP53):c.993+326_993+341del rs730882013
NM_001166108.2(PALLD):c.3359-24CT[5] rs536545858
NM_002354.2:c.1-45_1-26del
NM_002485.4:c.703-20insA
NM_004360.3:c.2164+17insA
NM_004655.4(AXIN2):c.-116-13del rs530658215
NM_004655.4(AXIN2):c.1200+18_1200+19delinsGC rs730881403
NM_005591.3:c.315-4insT
NM_005732.3:c.2923-5insT
NM_005732.4(RAD50):c.3476-18TTC[2] rs730881922
NM_005732.4(RAD50):c.756+7del rs377720482
NM_032043.3(BRIP1):c.1935+5GTT[2] rs730881641
NM_032043.3(BRIP1):c.380-17dup rs545021924

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