ClinVar Miner

List of variants in gene GAN reported as uncertain significance by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 74
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HGVS dbSNP gnomAD frequency
NM_022041.4(GAN):c.*1268C>T rs182391687 0.00845
NM_022041.4(GAN):c.1445C>T (p.Ala482Val) rs146576740 0.00169
NM_022041.4(GAN):c.*816T>C rs188599282 0.00144
NM_022041.4(GAN):c.1612+12A>G rs150344737 0.00135
NM_022041.4(GAN):c.*1336G>A rs150666164 0.00121
NM_022041.4(GAN):c.*495G>A rs558701236 0.00113
NM_022041.4(GAN):c.*1002T>A rs552489170 0.00107
NM_022041.4(GAN):c.*1029C>T rs189688967 0.00058
NM_022041.4(GAN):c.730A>G (p.Ile244Val) rs200749953 0.00051
NM_022041.4(GAN):c.*32C>A rs200964845 0.00048
NM_022041.4(GAN):c.973+6G>A rs372665411 0.00044
NM_022041.4(GAN):c.*1943T>C rs751490334 0.00039
NM_022041.4(GAN):c.*2532T>C rs528796667 0.00037
NM_022041.4(GAN):c.*1368T>C rs568868279 0.00031
NM_022041.4(GAN):c.*1138A>G rs554886016 0.00026
NM_022041.4(GAN):c.974-11G>C rs753746307 0.00026
NM_022041.4(GAN):c.*1883C>G rs76019247 0.00024
NM_022041.4(GAN):c.283-14T>C rs369700456 0.00019
NM_022041.4(GAN):c.1323T>C (p.Tyr441=) rs368072478 0.00011
NM_022041.4(GAN):c.944C>T (p.Pro315Leu) rs144486241 0.00011
NM_022041.4(GAN):c.*551C>T rs886052341 0.00010
NM_022041.4(GAN):c.1511A>G (p.Tyr504Cys) rs147864771 0.00010
NM_022041.4(GAN):c.1630G>A (p.Val544Met) rs200071978 0.00010
NM_022041.4(GAN):c.1199C>G (p.Thr400Ser) rs368571975 0.00009
NM_022041.4(GAN):c.*2019A>G rs886052347 0.00005
NM_022041.4(GAN):c.*810C>A rs886052342 0.00005
NM_022041.4(GAN):c.*2350T>A rs369040399 0.00004
NM_022041.4(GAN):c.1777C>T (p.Arg593Cys) rs886052336 0.00004
NM_022041.4(GAN):c.444C>T (p.His148=) rs764605890 0.00004
NM_022041.4(GAN):c.*544C>G rs141552591 0.00003
NM_022041.4(GAN):c.283-15A>G rs754182168 0.00003
NM_022041.4(GAN):c.*1557C>A rs528748555 0.00002
NM_022041.4(GAN):c.*1747A>G rs886052346 0.00002
NM_022041.4(GAN):c.*381G>A rs886052340 0.00002
NM_022041.4(GAN):c.1518C>T (p.Asn506=) rs886052333 0.00002
NM_022041.4(GAN):c.*1102A>G rs1394891003 0.00001
NM_022041.4(GAN):c.*2027T>A rs886052348 0.00001
NM_022041.4(GAN):c.*2492T>A rs886052354 0.00001
NM_022041.4(GAN):c.1017G>A (p.Gln339=) rs201451382 0.00001
NM_022041.4(GAN):c.1123A>T (p.Met375Leu) rs201252856 0.00001
NM_022041.4(GAN):c.1398T>C (p.Val466=) rs756485979 0.00001
NM_022041.4(GAN):c.1612+4A>G rs376218401 0.00001
NM_022041.4(GAN):c.471G>A (p.Leu157=) rs143704621 0.00001
NM_022041.4(GAN):c.572A>G (p.Asn191Ser) rs139748896 0.00001
NM_022041.4(GAN):c.634-6C>T rs199874705 0.00001
NM_022041.4(GAN):c.725G>A (p.Arg242Gln) rs371906996 0.00001
NM_022041.4(GAN):c.801A>G (p.Lys267=) rs746799355 0.00001
NM_022041.4(GAN):c.806G>A (p.Arg269Gln) rs759581558 0.00001
NM_022041.4(GAN):c.*1455del rs3214897
NM_022041.4(GAN):c.*1455dup rs3214897
NM_022041.4(GAN):c.*1585T>C rs886052344
NM_022041.4(GAN):c.*1659del rs546229255
NM_022041.4(GAN):c.*1670C>T rs569008014
NM_022041.4(GAN):c.*176G>T rs1196229669
NM_022041.4(GAN):c.*1820G>A rs561770690
NM_022041.4(GAN):c.*2125A>G rs1904295878
NM_022041.4(GAN):c.*214C>T rs886052338
NM_022041.4(GAN):c.*2280G>C rs886052349
NM_022041.4(GAN):c.*2332del rs533512036
NM_022041.4(GAN):c.*2332dup rs533512036
NM_022041.4(GAN):c.*2457T>C rs886052352
NM_022041.4(GAN):c.*2485A>G rs886052353
NM_022041.4(GAN):c.*291A>G rs541752526
NM_022041.4(GAN):c.*360G>A rs886052339
NM_022041.4(GAN):c.*360G>T rs886052339
NM_022041.4(GAN):c.*45T>C rs886052337
NM_022041.4(GAN):c.*644T>C rs1006920510
NM_022041.4(GAN):c.*733G>A rs530029543
NM_022041.4(GAN):c.-111G>A rs12929567
NM_022041.4(GAN):c.1183G>C (p.Asp395His) rs142456623
NM_022041.4(GAN):c.1665C>G (p.His555Gln) rs886052334
NM_022041.4(GAN):c.1699C>A (p.Arg567Ser) rs886052335
NM_022041.4(GAN):c.1783C>T (p.His595Tyr) rs757216350
NM_022041.4(GAN):c.440A>G (p.His147Arg) rs763438490

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