ClinVar Miner

List of variants in gene FLG reported as benign for autosomal dominant ichthyosis vulgaris

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 56
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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.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.10779G>C (p.Glu3593Asp) rs12083389 0.09982
NM_002016.2(FLG):c.10903G>A (p.Asp3635Asn) rs75448155 0.03325
NM_002016.2(FLG):c.4678C>T (p.Arg1560Cys) rs151103850 0.03042
NM_002016.2(FLG):c.9658G>C (p.Asp3220His) rs200240824 0.00179
NM_002016.2(FLG):c.10017G>A (p.Gln3339=)
NM_002016.2(FLG):c.10194T>C (p.Ser3398=)
NM_002016.2(FLG):c.10307G>C (p.Gly3436Ala)
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.11213G>A (p.Arg3738His)
NM_002016.2(FLG):c.2508T>C (p.Asp836=) rs3120653
NM_002016.2(FLG):c.2938C>G (p.His980Asp) rs12756586
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.5051G>A (p.Arg1684His)
NM_002016.2(FLG):c.5095C>T (p.Arg1699Cys)
NM_002016.2(FLG):c.5828T>A (p.Leu1943His) rs113544881
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.6058T>G (p.Ser2020Ala) rs7512857
NM_002016.2(FLG):c.6462A>C (p.Gln2154His) rs74129452
NM_002016.2(FLG):c.6990C>T (p.His2330=) rs6664985
NM_002016.2(FLG):c.7015G>A (p.Asp2339Asn)
NM_002016.2(FLG):c.7442T>C (p.Leu2481Ser) rs55650366
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.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.995G>T (p.Gly332Val)

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