ClinVar Miner

List of variants in gene SYNE2 reported as benign for not specified

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Gene type:
ClinVar version:
Total variants: 103
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HGVS dbSNP gnomAD frequency
NM_182914.3(SYNE2):c.8404A>G (p.Ser2802Gly) rs1890908 0.91221
NM_182914.3(SYNE2):c.7183G>A (p.Ala2395Thr) rs4027405 0.87610
NM_182914.3(SYNE2):c.6481C>T (p.Leu2161=) rs10151127 0.80823
NM_182914.3(SYNE2):c.7076G>A (p.Ser2359Asn) rs4027404 0.75629
NM_182914.3(SYNE2):c.9757G>C (p.Asp3253His) rs8010911 0.72882
NM_182914.3(SYNE2):c.6851C>T (p.Ala2284Val) rs4027402 0.72784
NM_182914.3(SYNE2):c.5906T>C (p.Met1969Thr) rs4902264 0.72634
NM_182914.3(SYNE2):c.8824A>G (p.Ile2942Val) rs3829767 0.71158
NM_182914.3(SYNE2):c.20062-119G>C rs1152588 0.66235
NM_182914.3(SYNE2):c.15556C>A (p.Leu5186Met) rs10151658 0.56664
NM_182914.3(SYNE2):c.19333+5C>T rs1152590 0.50736
NM_182914.3(SYNE2):c.17938T>C (p.Leu5980=) rs2256191 0.47326
NM_182914.3(SYNE2):c.15543C>T (p.Ile5181=) rs11629287 0.40212
NM_182914.3(SYNE2):c.17202C>A (p.Leu5734=) rs7161192 0.33500
NM_182914.3(SYNE2):c.4578-4T>A rs7146588 0.30679
NM_182914.3(SYNE2):c.19857G>T (p.Leu6619=) rs35648226 0.24610
NM_182914.3(SYNE2):c.399G>C (p.Leu133=) rs33976862 0.11557
NM_182914.3(SYNE2):c.11613A>G (p.Val3871=) rs17101637 0.10790
NM_182914.3(SYNE2):c.14844-5G>C rs17825431 0.10335
NM_182914.3(SYNE2):c.1721T>C (p.Ile574Thr) rs9944035 0.08879
NM_182914.3(SYNE2):c.12001T>C (p.Trp4001Arg) rs2792205 0.08782
NM_182914.3(SYNE2):c.12002G>A (p.Trp4001Ter) rs2781377 0.08740
NM_182914.3(SYNE2):c.6865T>C (p.Leu2289=) rs11850509 0.08174
NM_182914.3(SYNE2):c.9389A>G (p.Asn3130Ser) rs11847087 0.07400
NM_182914.3(SYNE2):c.4177C>T (p.Arg1393Trp) rs17751301 0.04972
NM_182914.3(SYNE2):c.14776T>C (p.Leu4926=) rs8007874 0.04106
NM_182914.3(SYNE2):c.7040C>A (p.Ala2347Glu) rs34625768 0.03914
NM_182914.3(SYNE2):c.7075A>G (p.Ser2359Gly) rs7157465 0.03914
NM_182914.3(SYNE2):c.4536A>G (p.Thr1512=) rs11158524 0.03853
NM_182914.3(SYNE2):c.14734C>G (p.Pro4912Ala) rs17766354 0.03286
NM_182914.3(SYNE2):c.3559A>C (p.Ile1187Leu) rs57259697 0.03281
NM_182914.3(SYNE2):c.2409C>A (p.Ser803=) rs17101525 0.03277
NM_182914.3(SYNE2):c.10567A>C (p.Lys3523Gln) rs35203186 0.03124
NM_182914.3(SYNE2):c.13423-7C>G rs7140414 0.03110
NM_182914.3(SYNE2):c.9078A>T (p.Glu3026Asp) rs34843668 0.02941
NM_182914.3(SYNE2):c.7690A>G (p.Ile2564Val) rs11628107 0.02936
NM_182914.3(SYNE2):c.12840+8T>C rs145218296 0.02317
NM_182914.3(SYNE2):c.12626T>C (p.Ile4209Thr) rs61747118 0.02309
NM_182914.3(SYNE2):c.13254C>A (p.Asn4418Lys) rs36021513 0.02290
NM_182914.3(SYNE2):c.11385G>A (p.Lys3795=) rs34954189 0.02196
NM_182914.3(SYNE2):c.1296C>A (p.Ser432Arg) rs35554503 0.02006
NM_182914.3(SYNE2):c.17556+4T>C rs2297301 0.01974
NM_182914.3(SYNE2):c.12122G>A (p.Arg4041His) rs17101661 0.01834
NM_182914.3(SYNE2):c.10269C>G (p.Ile3423Met) rs35920722 0.01612
NM_182914.3(SYNE2):c.8597C>T (p.Thr2866Met) rs114508894 0.01330
NM_182914.3(SYNE2):c.10196G>A (p.Arg3399His) rs36039501 0.01281
NM_182914.3(SYNE2):c.13266G>A (p.Gln4422=) rs34944385 0.01230
NM_182914.3(SYNE2):c.9023T>C (p.Ile3008Thr) rs115969845 0.01198
NM_182914.3(SYNE2):c.15794T>C (p.Val5265Ala) rs142660236 0.01196
NM_182914.3(SYNE2):c.14197C>A (p.Pro4733Thr) rs75568433 0.01070
NM_182914.3(SYNE2):c.16639G>A (p.Asp5547Asn) rs17179194 0.00998
NM_182914.3(SYNE2):c.19639A>G (p.Ile6547Val) rs45453691 0.00993
NM_182914.3(SYNE2):c.5187T>A (p.His1729Gln) rs116597541 0.00866
NM_182914.3(SYNE2):c.12596A>G (p.Asn4199Ser) rs35223918 0.00691
NM_182914.3(SYNE2):c.17561T>C (p.Leu5854Pro) rs117070973 0.00528
NM_182914.3(SYNE2):c.12378C>T (p.Ser4126=) rs36007735 0.00524
NM_182914.3(SYNE2):c.2803T>C (p.Leu935=) rs114718315 0.00474
NM_182914.3(SYNE2):c.7162G>A (p.Glu2388Lys) rs200842904 0.00462
NM_182914.3(SYNE2):c.6321C>T (p.Ser2107=) rs143410137 0.00434
NM_182914.3(SYNE2):c.18632C>T (p.Thr6211Met) rs36215895 0.00411
NM_182914.3(SYNE2):c.16420T>A (p.Ser5474Thr) rs114483901 0.00399
NM_182914.3(SYNE2):c.11379T>C (p.Leu3793=) rs149391344 0.00319
NM_182914.3(SYNE2):c.20117G>A (p.Arg6706Gln) rs35831865 0.00309
NM_182914.3(SYNE2):c.20596C>T (p.Leu6866=) rs141474837 0.00289
NM_182914.3(SYNE2):c.15781G>A (p.Val5261Ile) rs144605670 0.00267
NM_182914.3(SYNE2):c.20410G>A (p.Asp6804Asn) rs150644129 0.00259
NM_182914.3(SYNE2):c.12984A>G (p.Lys4328=) rs151314114 0.00255
NM_182914.3(SYNE2):c.10835A>G (p.Gln3612Arg) rs78110192 0.00249
NM_182914.3(SYNE2):c.19415C>T (p.Ser6472Leu) rs150955173 0.00242
NM_182914.3(SYNE2):c.16743G>A (p.Thr5581=) rs138769395 0.00232
NM_182914.3(SYNE2):c.20382+9A>G rs116394628 0.00230
NM_182914.3(SYNE2):c.20197G>A (p.Glu6733Lys) rs150172232 0.00181
NM_182914.3(SYNE2):c.8041G>A (p.Val2681Ile) rs150946074 0.00178
NM_182914.3(SYNE2):c.7898A>G (p.Asn2633Ser) rs190582637 0.00157
NM_182914.3(SYNE2):c.16156C>T (p.Leu5386Phe) rs184745422 0.00140
NM_182914.3(SYNE2):c.17388C>T (p.Pro5796=) rs35744699 0.00133
NM_182914.3(SYNE2):c.7163A>G (p.Glu2388Gly) rs45590135 0.00116
NM_182914.3(SYNE2):c.9347A>G (p.Lys3116Arg) rs138689053 0.00094
NM_182914.3(SYNE2):c.7124T>C (p.Leu2375Pro) rs111902869 0.00091
NM_182914.3(SYNE2):c.4842C>T (p.Pro1614=) rs148564084 0.00088
NM_182914.3(SYNE2):c.6690C>T (p.His2230=) rs138272705 0.00087
NM_182914.3(SYNE2):c.8403C>T (p.Gly2801=) rs189676726 0.00079
NM_182914.3(SYNE2):c.8964C>T (p.Leu2988=) rs374107455 0.00034
NM_182914.3(SYNE2):c.12043T>C (p.Tyr4015His) rs75665958 0.00029
NM_182914.3(SYNE2):c.7128A>G (p.Pro2376=) rs117423703 0.00029
NM_182914.3(SYNE2):c.990+10A>G rs145924910 0.00026
NM_182914.3(SYNE2):c.17723G>A (p.Arg5908His) rs538344879 0.00020
NM_182914.3(SYNE2):c.2013G>A (p.Leu671=) rs371320284 0.00014
NM_182914.3(SYNE2):c.9396G>C (p.Lys3132Asn) rs566182360 0.00009
NM_182914.3(SYNE2):c.3326G>A (p.Ser1109Asn) rs150464227 0.00007
NM_182914.3(SYNE2):c.5608A>C (p.Ser1870Arg) rs368227332 0.00001
NM_182914.3(SYNE2):c.9974C>T (p.Ala3325Val) rs377173620 0.00001
NM_182914.3(SYNE2):c.1129-4dup rs34440267
NM_182914.3(SYNE2):c.1129-6_1129-4del rs34440267
NM_182914.3(SYNE2):c.11944A>C (p.Asn3982His) rs10137972
NM_182914.3(SYNE2):c.11944A>G (p.Asn3982Asp) rs10137972
NM_182914.3(SYNE2):c.13707+10T>C rs61987277
NM_182914.3(SYNE2):c.20339G>A (p.Arg6780Gln) rs202240664
NM_182914.3(SYNE2):c.2070A>G (p.Leu690=) rs79037871
NM_182914.3(SYNE2):c.2647-3dup rs397726340
NM_182914.3(SYNE2):c.2647-4_2647-3dup rs397726340
NM_182914.3(SYNE2):c.4768G>T (p.Val1590Phe) rs1018808319
NM_182914.3(SYNE2):c.9926A>G (p.His3309Arg) rs8010699

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