ClinVar Miner

List of variants reported as benign for Focal segmental glomerulosclerosis 1

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Total variants: 41
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HGVS dbSNP gnomAD frequency
NM_004924.6(ACTN4):c.546C>T (p.Asn182=) rs3745859 0.39136
NM_004924.6(ACTN4):c.2563T>C (p.Leu855=) rs1136956 0.20720
NM_004924.6(ACTN4):c.1442+64C>T rs77822825 0.14962
NM_004924.6(ACTN4):c.537G>A (p.Pro179=) rs11553600 0.14941
NM_004924.6(ACTN4):c.278-98G>A rs73038909 0.14725
NM_004924.6(ACTN4):c.1291+81C>T rs7248577 0.05857
NM_004924.6(ACTN4):c.734-54C>T rs12984794 0.05568
NM_004924.6(ACTN4):c.1977T>C (p.Asn659=) rs12986337 0.05559
NM_004924.6(ACTN4):c.1551+49C>T rs62120068 0.05547
NM_004924.6(ACTN4):c.398-16C>T rs2287728 0.05415
NM_004924.6(ACTN4):c.652-37G>A rs45561939 0.04930
NM_004924.6(ACTN4):c.652-55G>T rs56737532 0.04927
NM_004924.6(ACTN4):c.820-94C>T rs2306196 0.03870
NM_004924.6(ACTN4):c.246C>T (p.Leu82=) rs77307137 0.02544
NM_004924.6(ACTN4):c.484+75C>T rs2368475 0.02543
NM_004924.6(ACTN4):c.1442+72C>T rs2306197 0.01470
NM_004924.6(ACTN4):c.929G>A (p.Arg310Gln) rs112545413 0.00927
NM_004924.6(ACTN4):c.369C>T (p.Gly123=) rs140381330 0.00875
NM_004924.6(ACTN4):c.1998G>A (p.Gln666=) rs145474119 0.00666
NM_004924.6(ACTN4):c.1611G>A (p.Ala537=) rs150183570 0.00498
NM_004924.6(ACTN4):c.2401G>A (p.Val801Met) rs141727248 0.00403
NM_004924.6(ACTN4):c.1218C>A (p.Arg406=) rs148259739 0.00334
NM_004924.6(ACTN4):c.1692+10C>G rs199619802 0.00300
NM_004924.6(ACTN4):c.536C>T (p.Pro179Leu) rs149027682 0.00270
NM_004924.6(ACTN4):c.978G>A (p.Gln326=) rs117392350 0.00253
NM_004924.6(ACTN4):c.1770C>T (p.Ile590=) rs140707871 0.00240
NM_004924.6(ACTN4):c.1608C>T (p.Arg536=) rs139575917 0.00232
NM_004924.6(ACTN4):c.1425C>T (p.Ala475=) rs144388375 0.00222
NM_004924.6(ACTN4):c.738C>T (p.Ile246=) rs34491236 0.00115
NM_004924.6(ACTN4):c.2016C>T (p.Ile672=) rs137985903 0.00110
NM_004924.6(ACTN4):c.2316G>A (p.Ala772=) rs192382222 0.00048
NM_004924.6(ACTN4):c.2191-5C>T rs186662077 0.00035
NM_004924.6(ACTN4):c.2679C>T (p.Pro893=) rs146493523 0.00033
NM_004924.6(ACTN4):c.2652G>A (p.Ala884=) rs202127035 0.00018
NM_004924.6(ACTN4):c.894C>T (p.Tyr298=) rs568574676 0.00016
NM_004924.6(ACTN4):c.1902C>T (p.Asp634=) rs139162351 0.00013
NM_004924.6(ACTN4):c.162+61T>C rs2303040
NM_004924.6(ACTN4):c.2418+28A>G rs12981131
NM_004924.6(ACTN4):c.2670C>A (p.Asp890Glu) rs113969422
NM_004924.6(ACTN4):c.277+29G>C rs2112649
NM_004924.6(ACTN4):c.652-34G>T rs58197765

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