ClinVar Miner

List of variants in gene TYK2 reported as benign for not provided

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Gene type:
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Total variants: 59
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HGVS dbSNP gnomAD frequency
NM_003331.5(TYK2):c.2908+31T>C rs280497 0.55677
NM_003331.5(TYK2):c.1669+7T>C rs280519 0.52527
NM_003331.5(TYK2):c.1368-237A>C rs91755 0.51793
NM_003331.5(TYK2):c.3200+122G>C rs280496 0.28843
NM_003331.5(TYK2):c.1477-6T>C rs280520 0.27974
NM_003331.5(TYK2):c.629+26T>C rs34725611 0.22818
NM_003331.5(TYK2):c.1084G>T (p.Val362Phe) rs2304256 0.22701
NM_003331.5(TYK2):c.-132T>C rs280500 0.19516
NM_003331.5(TYK2):c.1368-59C>T rs280521 0.17265
NM_003331.5(TYK2):c.1012-36C>T rs12720270 0.15757
NM_003331.5(TYK2):c.2467-171G>A rs12720307 0.12463
NM_003331.5(TYK2):c.2908+44T>C rs12720320 0.12252
NM_003331.5(TYK2):c.2048-315T>C rs12720293 0.12186
NM_003331.5(TYK2):c.2311+11G>C rs12720299 0.11734
NM_003331.5(TYK2):c.3318+150C>G rs12720326 0.11719
NM_003331.5(TYK2):c.2047+210C>T rs12720279 0.11326
NM_003331.5(TYK2):c.516C>T (p.Thr172=) rs280523 0.10217
NM_003331.5(TYK2):c.-20-69G>A rs12720222 0.10123
NM_003331.5(TYK2):c.3201-177G>T rs8100564 0.09252
NM_003331.5(TYK2):c.2175+152T>C rs12720294 0.09182
NM_003331.5(TYK2):c.317+26G>A rs6511696 0.08050
NM_003331.5(TYK2):c.2051T>G (p.Ile684Ser) rs12720356 0.06169
NM_003331.5(TYK2):c.465+48G>T rs12720253 0.05820
NM_003331.5(TYK2):c.1087G>A (p.Gly363Ser) rs2304255 0.05403
NM_003331.5(TYK2):c.629+21G>A rs79337061 0.05381
NM_003331.5(TYK2):c.2175+95T>C rs280516 0.04908
NM_003331.5(TYK2):c.2176-296A>G rs569002 0.04846
NM_003331.5(TYK2):c.465+191C>T rs35221071 0.04568
NM_003331.5(TYK2):c.2467-154C>T rs115469830 0.03069
NM_003331.5(TYK2):c.*134A>G rs12720334 0.03020
NM_003331.5(TYK2):c.3027+194C>A rs12720323 0.03015
NM_003331.5(TYK2):c.2617+206C>G rs12720309 0.03014
NM_003331.5(TYK2):c.2617+82G>T rs76148713 0.02989
NM_003331.5(TYK2):c.1367+185C>T rs10418513 0.02941
NM_003331.5(TYK2):c.2176-18C>G rs12720298 0.02818
NM_003331.5(TYK2):c.1848T>G (p.Pro616=) rs12720276 0.02503
NM_003331.5(TYK2):c.2617+257C>T rs12720311 0.02228
NM_003331.5(TYK2):c.2047+107A>G rs12720278 0.02174
NM_003331.5(TYK2):c.194-132C>T rs12720252 0.01738
NM_003331.5(TYK2):c.1953C>T (p.Ile651=) rs12720355 0.01009
NM_003331.5(TYK2):c.590G>A (p.Arg197His) rs12720263 0.00860
NM_003331.5(TYK2):c.942C>T (p.His314=) rs12720266 0.00844
NM_003331.5(TYK2):c.157G>A (p.Ala53Thr) rs55762744 0.00716
NM_003331.5(TYK2):c.114C>A (p.Gly38=) rs56295652 0.00377
NM_003331.5(TYK2):c.*146T>A rs145861532 0.00267
NM_003331.5(TYK2):c.2107C>T (p.Arg703Trp) rs55882956 0.00244
NM_003331.5(TYK2):c.3488A>G (p.Glu1163Gly) rs55886939 0.00226
NM_003331.5(TYK2):c.318-17G>A rs201764291 0.00017
NM_003331.5(TYK2):c.1011+222A>T rs12720354
NM_003331.5(TYK2):c.1368-331_1368-324del rs3074538
NM_003331.5(TYK2):c.1774-4G>C rs280518
NM_003331.5(TYK2):c.2175+100GTTT[3] rs143429818
NM_003331.5(TYK2):c.2311+16G>C rs12720300
NM_003331.5(TYK2):c.2467-48del rs12720308
NM_003331.5(TYK2):c.2617+211A>G rs12720310
NM_003331.5(TYK2):c.465+135del rs34301809
NM_003331.5(TYK2):c.466-154del rs750662938
NM_003331.5(TYK2):c.466-42G>T rs12720352
NM_003331.5(TYK2):c.629+97dup rs1310326387

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