List of variants reported as benign for immune system disorder by Counsyl

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Total variants: 26

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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_000243.3(MEFV):c.1764G>A (p.Pro588=)	rs1231122	0.41230
NM_000051.4(ATM):c.4777-20A>G	rs3218678	0.06221
NM_000051.4(ATM):c.186-17A>G	rs4987907	0.01587
NM_000051.4(ATM):c.3161C>G (p.Pro1054Arg)	rs1800057	0.01452
NM_002435.3(MPI):c.345+16C>T	rs143242949	0.01224
NM_058216.3(RAD51C):c.90G>A (p.Ala30=)	rs115414895	0.01193
NM_000051.4(ATM):c.6572+12G>T	rs3218677	0.01112
NM_000051.4(ATM):c.8419-19A>G	rs12279930	0.00824
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_000051.4(ATM):c.1176C>G (p.Gly392=)	rs1800727	0.00388
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_000051.4(ATM):c.497-4dup	rs768748099
NM_000051.4(ATM):c.8010+30dup	rs3218702
NM_058216.3(RAD51C):c.459T>G (p.Gly153=)	rs769486350

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