ClinVar Miner

List of variants reported as likely benign for Nephrotic syndrome by Illumina Clinical Services Laboratory,Illumina

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Total variants: 21
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HGVS dbSNP
NM_002292.4(LAMB2):c.1193C>T (p.Thr398Ile) rs77500937
NM_002292.4(LAMB2):c.1764C>T (p.Pro588=) rs33942096
NM_002292.4(LAMB2):c.2740G>A (p.Gly914Arg) rs35713889
NM_002292.4(LAMB2):c.2959G>A (p.Glu987Lys) rs34759087
NM_002292.4(LAMB2):c.306C>T (p.Asn102=) rs79448908
NM_002292.4(LAMB2):c.3387A>G (p.Gln1129=) rs34290943
NM_002292.4(LAMB2):c.4774C>T (p.Arg1592Trp) rs61729458
NM_002292.4(LAMB2):c.5293G>A (p.Ala1765Thr) rs74951356
NM_016341.4(PLCE1):c.*166G>C rs11187870
NM_016341.4(PLCE1):c.*253C>T rs79412094
NM_016341.4(PLCE1):c.*28A>G rs3203713
NM_016341.4(PLCE1):c.-525T>C rs75639609
NM_016341.4(PLCE1):c.1405T>A (p.Ser469Thr) rs17508082
NM_016341.4(PLCE1):c.2124G>A (p.Val708=) rs61751496
NM_016341.4(PLCE1):c.2352C>T (p.Asp784=) rs201793869
NM_016341.4(PLCE1):c.3132C>T (p.His1044=) rs61732522
NM_016341.4(PLCE1):c.4059C>T (p.Phe1353=) rs61751499
NM_016341.4(PLCE1):c.4263G>A (p.Ser1421=) rs41291134
NM_016341.4(PLCE1):c.5458+7G>A rs17516758
NM_016341.4(PLCE1):c.5669C>T (p.Pro1890Leu) rs58539480
NM_016341.4(PLCE1):c.6342+13G>A rs75283731

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