List of variants reported as uncertain significance for immune system disorder by Clinical Genomics, Uppaluri K&H Personalized Medicine Clinic

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_012275.3(IL36RN):c.*276A>G	rs1800930	0.64674
NM_012275.3(IL36RN):c.*418A>G	rs3180235	0.64649
NM_012275.3(IL36RN):c.*560C>G	rs2472188	0.64649
NM_012275.3(IL36RN):c.*222T>C	rs2515401	0.64643
NM_012275.3(IL36RN):c.*326C>A	rs2515402	0.64633
NM_000207.3(INS):c.*22A>C	rs3842753	0.59307
NM_014009.4(FOXP3):c.543C>T (p.Ser181=)	rs2232367	0.03006
NM_001715.3(BLK):c.1057C>T (p.Arg353Cys)	rs199696853	0.00006
NM_000207.3(INS):c.67G>A (p.Ala23Thr)	rs13306444
NM_012275.3(IL36RN):c.*401A>T	rs3180234

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