List of variants reported as benign for bone marrow disorder by Counsyl

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Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_032043.3(BRIP1):c.2637A>G (p.Glu879=)	rs4986765	0.74166
NM_032043.3(BRIP1):c.2755T>C (p.Ser919Pro)	rs4986764	0.61453
NM_032043.3(BRIP1):c.3411T>C (p.Tyr1137=)	rs4986763	0.60694
NM_058216.3(RAD51C):c.90G>A (p.Ala30=)	rs115414895	0.01193
NM_032043.3(BRIP1):c.206-21T>C	rs2048717	0.00589
NM_032043.3(BRIP1):c.1141-94G>T	rs114901675	0.00573
NM_032043.3(BRIP1):c.2236A>G (p.Ile746Val)	rs111536363	0.00480
NM_058216.3(RAD51C):c.186A>G (p.Gln62=)	rs28363303	0.00322
NM_032043.3(BRIP1):c.577G>A (p.Val193Ile)	rs4988346	0.00305
NM_058216.3(RAD51C):c.195A>G (p.Arg65=)	rs45511291	0.00105
NM_032043.3(BRIP1):c.2257+19A>C	rs77851913	0.00079
NM_032043.3(BRIP1):c.918+15T>A	rs117820198	0.00078
NM_058216.3(RAD51C):c.146-8A>G	rs201079501	0.00074
NM_032043.3(BRIP1):c.430G>A (p.Ala144Thr)	rs116952709	0.00055
NM_032043.3(BRIP1):c.1433A>G (p.His478Arg)	rs45501097	0.00002
NM_058216.3(RAD51C):c.459T>G (p.Gly153=)	rs769486350

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