ClinVar Miner

List of variants in gene RTTN reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 128
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_173630.4(RTTN):c.3384-226C>G rs74999746 0.02084
NM_173630.4(RTTN):c.4302+112C>T rs17232744 0.02056
NM_173630.4(RTTN):c.3384-303G>C rs17233212 0.02039
NM_173630.4(RTTN):c.398-257C>T rs3851131 0.01999
NM_173630.4(RTTN):c.2173-289C>T rs74679198 0.01951
NM_173630.4(RTTN):c.2886-184C>T rs147260916 0.01739
NM_173630.4(RTTN):c.1930-273A>G rs113475449 0.01716
NM_173630.4(RTTN):c.220-34A>G rs113341500 0.01299
NM_173630.4(RTTN):c.487+220G>A rs118090440 0.01241
NM_173630.4(RTTN):c.4654-175A>T rs74989897 0.01190
NM_173630.4(RTTN):c.398-221A>C rs149769355 0.01175
NM_173630.4(RTTN):c.6525+325C>G rs79010619 0.01112
NM_173630.4(RTTN):c.5951-57T>C rs150783273 0.01098
NM_173630.4(RTTN):c.1803-320G>A rs116391038 0.00990
NM_173630.4(RTTN):c.5647+100del rs148044924 0.00975
NM_173630.4(RTTN):c.6595+221T>C rs150138947 0.00946
NM_173630.4(RTTN):c.2481+166dup rs202065572 0.00917
NM_173630.4(RTTN):c.1690-305C>T rs141377528 0.00892
NM_173630.4(RTTN):c.2310-206A>C rs141390999 0.00887
NM_173630.4(RTTN):c.6526-221A>G rs138797734 0.00847
NM_173630.4(RTTN):c.841+11T>C rs114480216 0.00778
NM_173630.4(RTTN):c.1008-137C>T rs115425050 0.00776
NM_173630.4(RTTN):c.3143+211G>A rs79547006 0.00737
NM_173630.4(RTTN):c.5648-124A>G rs116226189 0.00737
NM_173630.4(RTTN):c.1690-228G>C rs114076061 0.00731
NM_173630.4(RTTN):c.6525+151C>A rs73970810 0.00726
NM_173630.4(RTTN):c.4374+116G>A rs13381186 0.00718
NM_173630.4(RTTN):c.2582-291A>G rs74983640 0.00713
NM_173630.4(RTTN):c.2309+240T>C rs150941646 0.00684
NM_173630.4(RTTN):c.6445G>A (p.Ala2149Thr) rs34989098 0.00624
NM_173630.4(RTTN):c.6421+158C>G rs186533402 0.00613
NM_173630.4(RTTN):c.4565-148T>A rs541151394 0.00606
NM_173630.4(RTTN):c.1803-241A>C rs73966815 0.00597
NM_173630.4(RTTN):c.841+160G>A rs114476702 0.00588
NM_173630.4(RTTN):c.4303-159C>T rs74906380 0.00583
NM_173630.4(RTTN):c.1929+87T>G rs79820873 0.00564
NM_173630.4(RTTN):c.3903+241G>A rs115590724 0.00563
NM_173630.4(RTTN):c.488-185A>G rs146893606 0.00558
NM_173630.4(RTTN):c.6595+138A>G rs115029214 0.00556
NM_173630.4(RTTN):c.579-139A>G rs116599744 0.00547
NM_173630.4(RTTN):c.4654-51T>G rs114066125 0.00543
NM_173630.4(RTTN):c.2582-277G>A rs76112951 0.00541
NM_173630.4(RTTN):c.5647+16C>T rs114315958 0.00541
NM_173630.4(RTTN):c.3904-49T>A rs116195581 0.00537
NM_173630.4(RTTN):c.1306-205T>A rs187658749 0.00536
NM_173630.4(RTTN):c.5648-87C>G rs115926328 0.00534
NM_173630.4(RTTN):c.1008-130G>A rs80320654 0.00533
NM_173630.4(RTTN):c.1189+56G>A rs77842988 0.00533
NM_173630.4(RTTN):c.693+90A>T rs115744565 0.00533
NM_173630.4(RTTN):c.693+143A>G rs74573462 0.00532
NM_173630.4(RTTN):c.5323+303A>G rs150562794 0.00480
NM_173630.4(RTTN):c.3903+262G>A rs116279002 0.00475
NM_173630.4(RTTN):c.2309+12G>A rs144279235 0.00433
NM_173630.4(RTTN):c.2788+317A>G rs139342442 0.00412
NM_173630.4(RTTN):c.5185+27T>C rs115817045 0.00401
NM_173630.4(RTTN):c.2055+133T>C rs78448243 0.00389
NM_173630.4(RTTN):c.4032+223C>G rs142434780 0.00354
NM_173630.4(RTTN):c.635A>C (p.Asp212Ala) rs12956068 0.00334
NM_173630.4(RTTN):c.397+134G>T rs78355766 0.00321
NM_173630.4(RTTN):c.694-273C>T rs115043430 0.00314
NM_173630.4(RTTN):c.3143+44T>C rs114887246 0.00309
NM_173630.4(RTTN):c.5823+118C>T rs117339348 0.00298
NM_173630.4(RTTN):c.5143A>G (p.Asn1715Asp) rs35374168 0.00275
NM_173630.4(RTTN):c.2954+106A>G rs78075144 0.00258
NM_173630.4(RTTN):c.4193C>T (p.Thr1398Met) rs62089120 0.00216
NM_173630.4(RTTN):c.5212C>T (p.His1738Tyr) rs35068710 0.00210
NM_173630.4(RTTN):c.5280G>A (p.Pro1760=) rs186543005 0.00198
NM_173630.4(RTTN):c.1330G>A (p.Gly444Arg) rs199780405 0.00192
NM_173630.4(RTTN):c.5883G>A (p.Leu1961=) rs35313369 0.00185
NM_173630.4(RTTN):c.4303-50C>T rs547433762 0.00164
NM_173630.4(RTTN):c.3003C>T (p.Tyr1001=) rs200031043 0.00156
NM_173630.4(RTTN):c.1563T>C (p.Ile521=) rs200975487 0.00148
NM_173630.4(RTTN):c.4308A>G (p.Ala1436=) rs200315704 0.00115
NM_173630.4(RTTN):c.885A>G (p.Ala295=) rs148445363 0.00111
NM_173630.4(RTTN):c.805T>C (p.Phe269Leu) rs141156594 0.00096
NM_173630.4(RTTN):c.841+26C>T rs201108414 0.00086
NM_173630.4(RTTN):c.1221A>G (p.Glu407=) rs112327299 0.00081
NM_173630.4(RTTN):c.4748-7A>G rs141673274 0.00063
NM_173630.4(RTTN):c.2568T>A (p.Ala856=) rs370998068 0.00061
NM_173630.4(RTTN):c.282G>T (p.Arg94=) rs199908033 0.00057
NM_173630.4(RTTN):c.4032+6C>T rs182157946 0.00048
NM_173630.4(RTTN):c.4654-43C>T rs189834726 0.00034
NM_173630.4(RTTN):c.3783G>A (p.Pro1261=) rs371484273 0.00032
NM_173630.4(RTTN):c.-26C>T rs374176554 0.00030
NM_173630.4(RTTN):c.1831C>T (p.Leu611=) rs372717287 0.00029
NM_173630.4(RTTN):c.2355T>C (p.Ser785=) rs200600259 0.00029
NM_173630.4(RTTN):c.488-15C>T rs182610959 0.00029
NM_173630.4(RTTN):c.86T>C (p.Ile29Thr) rs201689582 0.00021
NM_173630.4(RTTN):c.494A>C (p.Gln165Pro) rs199536536 0.00019
NM_173630.4(RTTN):c.708G>T (p.Leu236=) rs201505457 0.00017
NM_173630.4(RTTN):c.2670+9A>G rs200758402 0.00016
NM_173630.4(RTTN):c.4707A>T (p.Thr1569=) rs143709749 0.00015
NM_173630.4(RTTN):c.5055A>G (p.Leu1685=) rs372431222 0.00014
NM_173630.4(RTTN):c.2481+18G>T rs746996156 0.00012
NM_173630.4(RTTN):c.5850C>T (p.Val1950=) rs370480126 0.00012
NM_173630.4(RTTN):c.4564+4A>C rs368489465 0.00009
NM_173630.4(RTTN):c.3084A>G (p.Ser1028=) rs764877763 0.00006
NM_173630.4(RTTN):c.4253T>C (p.Val1418Ala) rs376967382 0.00006
NM_173630.4(RTTN):c.4877C>T (p.Thr1626Met) rs781683199 0.00006
NM_173630.4(RTTN):c.1305+11A>G rs547572919 0.00003
NM_173630.4(RTTN):c.1768C>T (p.Leu590=) rs752422245 0.00003
NM_173630.4(RTTN):c.2789-11T>G rs1258727329 0.00001
NM_173630.4(RTTN):c.4932T>G (p.Leu1644=) rs1057521884 0.00001
NM_173630.4(RTTN):c.5647+10A>G rs1057523916 0.00001
NC_000018.10:g.70205914del rs200984342
NM_173630.4(RTTN):c.1476+295_1476+298del rs372590513
NM_173630.4(RTTN):c.2055+33G>C rs116715798
NM_173630.4(RTTN):c.27A>G (p.Lys9=) rs1555784718
NM_173630.4(RTTN):c.2955-174del rs142593943
NM_173630.4(RTTN):c.3143+144C>A rs116794642
NM_173630.4(RTTN):c.3157T>C (p.Leu1053=) rs1599682423
NM_173630.4(RTTN):c.3321G>A (p.Lys1107=) rs147728279
NM_173630.4(RTTN):c.3384-4A>G rs1455491554
NM_173630.4(RTTN):c.4033-158_4033-157del rs139499965
NM_173630.4(RTTN):c.4303-21_4303-11del rs531741265
NM_173630.4(RTTN):c.4303-28_4303-11del rs531741265
NM_173630.4(RTTN):c.4565-125C>G rs73964495
NM_173630.4(RTTN):c.4565-6_4565-4del rs775033795
NM_173630.4(RTTN):c.5323+7_5323+9del rs770541694
NM_173630.4(RTTN):c.5745+205A>G rs142318554
NM_173630.4(RTTN):c.5745+27TA[2] rs200091480
NM_173630.4(RTTN):c.6339C>T (p.His2113=) rs1201086381
NM_173630.4(RTTN):c.6417T>C (p.Ala2139=) rs141934309
NM_173630.4(RTTN):c.6595+165_6595+168del rs545009598
NM_173630.4(RTTN):c.6596-278A>G rs145054997
NM_173630.4(RTTN):c.693+330C>G rs79226724
NM_173630.4(RTTN):c.693+38G>C rs116130278
NM_173630.4(RTTN):c.694-74T>G rs79879463

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.