ClinVar Miner

List of variants in gene GAN reported as benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 65
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HGVS dbSNP gnomAD frequency
NM_022041.3(GAN):c.-323G>T rs12599564 0.90188
NM_022041.4(GAN):c.974-303C>T rs2608552 0.89538
NM_022041.4(GAN):c.1236+256T>C rs9935709 0.66150
NM_022041.4(GAN):c.1237-59G>A rs4889313 0.64331
NM_022041.4(GAN):c.*472C>G rs1816122 0.61663
NM_022041.4(GAN):c.*592T>A rs1345895 0.59860
NM_022041.4(GAN):c.*247G>A rs2216769 0.57491
NM_022041.4(GAN):c.283-283A>G rs729181 0.47758
NM_022041.4(GAN):c.*967G>A rs12920236 0.41705
NM_022041.4(GAN):c.282+223C>T rs9938148 0.41322
NM_022041.4(GAN):c.1502+222G>A rs2615701 0.23571
NM_022041.4(GAN):c.1087-233T>C rs2550738 0.21940
NM_022041.4(GAN):c.1293C>T (p.Tyr431=) rs2608555 0.21491
NM_022041.4(GAN):c.1087-161T>C rs9933250 0.20409
NM_022041.4(GAN):c.1086+71C>T rs12448327 0.18756
NM_022041.4(GAN):c.1237-261G>A rs9930065 0.15179
NM_022041.4(GAN):c.*2188T>C rs2290949 0.09906
NM_022041.4(GAN):c.*235T>C rs16955203 0.09324
NM_022041.4(GAN):c.*1817G>C rs73602873 0.05804
NM_022041.4(GAN):c.*764G>A rs1934 0.05779
NM_022041.4(GAN):c.*227G>A rs113970605 0.05772
NM_022041.4(GAN):c.*1658T>G rs16955221 0.05141
NM_022041.4(GAN):c.*1068T>G rs57170812 0.05139
NM_022041.4(GAN):c.*1250T>G rs61096092 0.05139
NM_022041.4(GAN):c.1503-320A>G rs73602865 0.05136
NM_022041.4(GAN):c.*1388A>G rs41484544 0.05121
NM_022041.4(GAN):c.168-147A>G rs16955109 0.04233
NM_022041.4(GAN):c.*2498T>G rs2290948 0.04199
NM_022041.4(GAN):c.*294A>G rs16955210 0.04160
NM_022041.4(GAN):c.851+125T>C rs113656513 0.04087
NM_022041.4(GAN):c.168-66G>A rs9935105 0.03562
NM_022041.4(GAN):c.*81T>C rs78835723 0.03196
NM_022041.4(GAN):c.*2322T>G rs11862952 0.02277
NM_022041.4(GAN):c.973+148G>A rs7191388 0.02272
NM_022041.4(GAN):c.1087-225T>A rs112859650 0.02102
NM_022041.4(GAN):c.634-51T>C rs56859781 0.02004
NM_022041.4(GAN):c.*1908A>C rs11861082 0.01673
NM_022041.4(GAN):c.*1273G>C rs75176423 0.01472
NM_022041.4(GAN):c.*159C>T rs76000455 0.01456
NM_022041.4(GAN):c.1612+13C>G rs80326128 0.00917
NM_022041.4(GAN):c.*1268C>T rs182391687 0.00845
NM_022041.4(GAN):c.1239C>T (p.Ile413=) rs61740238 0.00609
NM_022041.4(GAN):c.168-48C>G rs77078389 0.00453
NM_022041.4(GAN):c.*1113G>A rs114880082 0.00415
NM_022041.4(GAN):c.1684C>G (p.Pro562Ala) rs79901179 0.00388
NM_022041.4(GAN):c.*372G>A rs79192026 0.00361
NM_022041.4(GAN):c.1182C>T (p.Tyr394=) rs150102659 0.00357
NM_022041.4(GAN):c.1502+11A>G rs143413333 0.00263
NM_022041.4(GAN):c.633+19A>G rs112194888 0.00138
NM_022041.4(GAN):c.1612+12A>G rs150344737 0.00135
NM_022041.4(GAN):c.1162C>T (p.Leu388=) rs73589395 0.00103
NM_022041.4(GAN):c.283-20T>C rs371984923 0.00093
NM_022041.4(GAN):c.974-11G>C rs753746307 0.00026
NM_022041.4(GAN):c.634-15T>C rs367608270 0.00013
NM_022041.4(GAN):c.1373+18G>A rs187260981 0.00006
NM_022041.4(GAN):c.*1659del rs546229255
NM_022041.4(GAN):c.*237T>A rs113064319
NM_022041.4(GAN):c.1086+25_1086+28del rs561109989
NM_022041.4(GAN):c.1086+51C>T rs78861333
NM_022041.4(GAN):c.1087-314dup rs35727292
NM_022041.4(GAN):c.168-12dup
NM_022041.4(GAN):c.1728G>C (p.Ala576=) rs150342446
NM_022041.4(GAN):c.282+7_282+9del rs563977770
NM_022041.4(GAN):c.283-149del rs5818329
NM_022041.4(GAN):c.974-186A>G rs8055288

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