ClinVar Miner

List of variants in gene FLG reported as benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 109
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HGVS dbSNP gnomAD frequency
NM_002016.2(FLG):c.6580T>C (p.Tyr2194His) rs2184953 0.36718
NM_002016.2(FLG):c.3500C>G (p.Ala1167Gly) rs58001094 0.36345
NM_002016.2(FLG):c.10473T>C (p.Asn3491=) rs3126067 0.35326
NM_002016.2(FLG):c.7633G>A (p.Gly2545Arg) rs3126072 0.30247
NM_002016.2(FLG):c.6498T>C (p.Ser2166=) rs2184954 0.29665
NM_002016.2(FLG):c.1360A>G (p.Thr454Ala) rs2011331 0.29513
NM_002016.2(FLG):c.3387T>C (p.Ser1129=) rs66831674 0.29380
NM_002016.2(FLG):c.7521C>G (p.His2507Gln) rs3126074 0.29374
NM_002016.2(FLG):c.10491T>C (p.Asp3497=) rs3126066 0.28029
NM_002016.2(FLG):c.4079G>A (p.Arg1360His) rs11586631 0.24233
NM_002016.2(FLG):c.6355T>C (p.Tyr2119His) rs7512553 0.22529
NM_002016.2(FLG):c.6354T>C (p.His2118=) rs7512554 0.22510
NM_002016.2(FLG):c.6323C>T (p.Ala2108Val) rs7522925 0.22487
NM_002016.2(FLG):c.6072T>C (p.His2024=) rs80353812 0.22174
NM_002016.2(FLG):c.6134G>C (p.Ser2045Thr) rs7546186 0.21962
NM_002016.2(FLG):c.8673G>T (p.Val2891=) rs57672167 0.21698
NM_002016.2(FLG):c.6891G>C (p.Glu2297Asp) rs78179835 0.19546
NM_002016.2(FLG):c.1432C>T (p.Pro478Ser) rs11584340 0.18876
NM_002016.2(FLG):c.7330A>G (p.Lys2444Glu) rs71625200 0.18787
NM_002016.2(FLG):c.9966A>G (p.Gln3322=) rs6681433 0.18589
NM_002016.2(FLG):c.2263G>A (p.Glu755Lys) rs74129461 0.16950
NM_002016.2(FLG):c.7192G>C (p.Glu2398Gln) rs71625201 0.16907
NM_002016.2(FLG):c.8807A>G (p.Asp2936Gly) rs80221306 0.14878
NM_002016.2(FLG):c.5414C>T (p.Ala1805Val) rs12405241 0.14180
NM_002016.2(FLG):c.5672G>A (p.Arg1891Gln) rs12407748 0.14161
NM_002016.2(FLG):c.1330G>A (p.Gly444Arg) rs11588170 0.14153
NM_002016.2(FLG):c.7097G>C (p.Ser2366Thr) rs71625202 0.13600
NM_002016.2(FLG):c.3551C>T (p.Ser1184Leu) rs3120649 0.10643
NM_002016.2(FLG):c.11803T>C (p.Ser3935Pro) rs3126065 0.10605
NM_002016.2(FLG):c.6190A>C (p.Lys2064Gln) rs74129455 0.10140
NM_002016.2(FLG):c.10779G>C (p.Glu3593Asp) rs12083389 0.09982
NM_002016.2(FLG):c.6455C>A (p.Ser2152Tyr) rs77249082 0.08035
NM_002016.2(FLG):c.4463C>A (p.Thr1488Asn) rs3120648 0.07460
NM_002016.2(FLG):c.6226G>A (p.Ala2076Thr) rs78125326 0.06078
NM_002016.2(FLG):c.10691G>T (p.Arg3564Leu) rs7518080 0.04576
NM_002016.2(FLG):c.1322G>A (p.Gly441Glu) rs76955400 0.03851
NM_002016.2(FLG):c.10903G>A (p.Asp3635Asn) rs75448155 0.03325
NM_002016.2(FLG):c.*179C>T rs12071181 0.03122
NM_002016.2(FLG):c.4678C>T (p.Arg1560Cys) rs151103850 0.03042
NM_002016.2(FLG):c.9520A>G (p.Ser3174Gly) rs74925349 0.02874
NM_002016.2(FLG):c.11485C>T (p.Arg3829Cys) rs7537147 0.02482
NM_002016.2(FLG):c.138+202A>T rs115170236 0.02482
NM_002016.2(FLG):c.5448C>G (p.His1816Gln) rs12073613 0.02473
NM_002016.2(FLG):c.5703C>T (p.Gly1901=) rs12073518 0.02455
NM_002016.2(FLG):c.7992C>G (p.Ser2664Arg) rs541212199 0.01730
NM_002016.2(FLG):c.10055C>G (p.Thr3352Arg) rs149573489 0.01607
NM_002016.2(FLG):c.4222C>A (p.Gln1408Lys) rs141177690 0.01604
NM_002016.2(FLG):c.5617C>A (p.Gln1873Lys) rs62623409 0.01581
NM_002016.2(FLG):c.4568C>T (p.Thr1523Ile) rs12750081 0.01579
NM_002016.2(FLG):c.4410T>C (p.His1470=) rs12732920 0.01567
NM_002016.2(FLG):c.7398G>A (p.Pro2466=) rs71625199 0.01563
NM_002016.2(FLG):c.6045C>A (p.Asp2015Glu) rs71626704 0.01554
NM_002016.2(FLG):c.6787G>A (p.Ala2263Thr) rs150947632 0.01542
NM_002016.2(FLG):c.8750G>T (p.Gly2917Val) rs146487738 0.01462
NM_002016.2(FLG):c.6218A>G (p.Lys2073Arg) rs147095782 0.01381
NM_002016.2(FLG):c.2539T>A (p.Ser847Thr) rs74129459 0.01342
NM_002016.2(FLG):c.11909C>T (p.Ser3970Leu) rs3814299 0.01144
NM_002016.2(FLG):c.4533G>C (p.Arg1511Ser) rs138596526 0.01016
NM_002016.2(FLG):c.9262G>A (p.Gly3088Arg) rs75985828 0.00989
NM_002016.2(FLG):c.6671T>A (p.Leu2224Gln) rs117945779 0.00754
NM_002016.2(FLG):c.10735A>G (p.Thr3579Ala) rs140128255 0.00575
NM_002016.2(FLG):c.10734C>T (p.Pro3578=) rs527359114 0.00568
NM_002016.2(FLG):c.6674T>C (p.Val2225Ala) rs116918835 0.00215
NM_002016.2(FLG):c.6675G>A (p.Val2225=) rs564482396 0.00209
NM_002016.2(FLG):c.10278G>A (p.Ala3426=) rs146896940
NM_002016.2(FLG):c.10590G>T (p.Arg3530Ser) rs72697000
NM_002016.2(FLG):c.10663T>C (p.Trp3555Arg) rs12728605
NM_002016.2(FLG):c.10691G>A (p.Arg3564His) rs7518080
NM_002016.2(FLG):c.10703A>G (p.Gln3568Arg) rs7532285
NM_002016.2(FLG):c.10736C>G (p.Thr3579Arg) rs3126075
NM_002016.2(FLG):c.10764C>T (p.His3588=) rs12742178
NM_002016.2(FLG):c.10985G>C (p.Ser3662Thr) rs75235053
NM_002016.2(FLG):c.138+40_138+42del rs112911800
NM_002016.2(FLG):c.139-119del rs34224823
NM_002016.2(FLG):c.139-84G>C rs3126082
NM_002016.2(FLG):c.2508T>C (p.Asp836=) rs3120653
NM_002016.2(FLG):c.2689C>T (p.Arg897Cys) rs76586335
NM_002016.2(FLG):c.2938C>G (p.His980Asp) rs12756586
NM_002016.2(FLG):c.3419G>A (p.Arg1140Gln) rs146853599
NM_002016.2(FLG):c.4126A>G (p.Arg1376Gly) rs11581433
NM_002016.2(FLG):c.4445C>A (p.Ser1482Tyr) rs11204978
NM_002016.2(FLG):c.4452C>G (p.Asp1484Glu) rs71626706
NM_002016.2(FLG):c.5839T>G (p.Trp1947Gly) rs80059102
NM_002016.2(FLG):c.5883C>A (p.His1961Gln) rs3126079
NM_002016.2(FLG):c.5896G>A (p.Gly1966Ser) rs111661820
NM_002016.2(FLG):c.6058T>G (p.Ser2020Ala) rs7512857
NM_002016.2(FLG):c.6462A>C (p.Gln2154His) rs74129452
NM_002016.2(FLG):c.6574A>C (p.Lys2192Gln) rs66954353
NM_002016.2(FLG):c.6603T>C (p.Asp2201=) rs2338554
NM_002016.2(FLG):c.6626A>G (p.His2209Arg) rs66977240
NM_002016.2(FLG):c.6697C>T (p.Pro2233Ser) rs554101492
NM_002016.2(FLG):c.6716G>A (p.Arg2239Gln) rs146612963
NM_002016.2(FLG):c.6990C>T (p.His2330=) rs6664985
NM_002016.2(FLG):c.7442T>C (p.Leu2481Ser) rs55650366
NM_002016.2(FLG):c.7956A>C (p.Glu2652Asp) rs192116923
NM_002016.2(FLG):c.8343C>T (p.Asp2781=) rs57670307
NM_002016.2(FLG):c.8506A>C (p.Ser2836Arg) rs11582087
NM_002016.2(FLG):c.8548G>A (p.Gly2850Ser) rs2184952
NM_002016.2(FLG):c.8768T>G (p.Leu2923Arg) rs144520421
NM_002016.2(FLG):c.8878G>A (p.Gly2960Ser) rs61690342
NM_002016.2(FLG):c.8928A>C (p.Glu2976Asp) rs61816760
NM_002016.2(FLG):c.9115T>C (p.Ser3039Pro) rs544832484
NM_002016.2(FLG):c.9117C>G (p.Ser3039=) rs779847367
NM_002016.2(FLG):c.9125A>G (p.Gln3042Arg) rs531404583
NM_002016.2(FLG):c.9313T>G (p.Tyr3105Asp) rs2065958
NM_002016.2(FLG):c.9536T>G (p.Val3179Gly) rs2065957
NM_002016.2(FLG):c.9540A>G (p.Ser3180=) rs3126069
NM_002016.2(FLG):c.9645G>T (p.Val3215=) rs9436066
NM_002016.2(FLG):c.974C>T (p.Ala325Val) rs75429799

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