ClinVar Miner

List of variants reported as benign for Immunodeficiency 51 by Illumina Laboratory Services, Illumina

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Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_014339.7(IL17RA):c.*249A>C rs5994164 0.02803
NM_014339.7(IL17RA):c.2295G>A (p.Gln765=) rs41482444 0.02725
NM_014339.7(IL17RA):c.*3060A>G rs12157837 0.02397
NM_014339.7(IL17RA):c.*5256C>T rs1003944 0.01864
NM_014339.7(IL17RA):c.*5270C>T rs1003943 0.01714
NM_014339.7(IL17RA):c.*5659G>A rs7289055 0.01147
NM_014339.7(IL17RA):c.*5036C>T rs1003945 0.01136
NM_014339.7(IL17RA):c.1819G>A (p.Glu607Lys) rs28376631 0.00845
NM_014339.7(IL17RA):c.*238G>C rs143922111 0.00671
NM_014339.7(IL17RA):c.*2112C>T rs12159073 0.00663
NM_014339.7(IL17RA):c.*1379A>T rs5992627 0.00655
NM_014339.7(IL17RA):c.*2111C>T rs114684847 0.00510
NM_014339.7(IL17RA):c.1747G>C (p.Asp583His) rs41432148 0.00389
NM_014339.7(IL17RA):c.833G>A (p.Arg278His) rs141467790 0.00070
NM_014339.7(IL17RA):c.2389A>G (p.Ile797Val) rs74827998 0.00018
NM_014339.7(IL17RA):c.*2163G>C rs543545127 0.00013
NM_014339.7(IL17RA):c.*3976G>A rs576803215 0.00009
NM_014339.7(IL17RA):c.*2066G>C rs375958748 0.00005
NM_014339.7(IL17RA):c.*3624G>A rs563135481 0.00005
NM_014339.6(IL17RA):c.-126C>G rs562165706
NM_014339.7(IL17RA):c.*803G>A rs12158721
NM_014339.7(IL17RA):c.-33C>G rs41525344
NM_014339.7(IL17RA):c.138+12C>T rs534287611

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