ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 80
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HGVS dbSNP
NM_032578.3(MYPN):c.1079-131A>G rs16925151
NM_032578.3(MYPN):c.1079-215G>T rs2673800
NM_032578.3(MYPN):c.1079-296T>C rs148463826
NM_032578.3(MYPN):c.1079-39T>A rs114286560
NM_032578.3(MYPN):c.1130+132C>T rs2635993
NM_032578.3(MYPN):c.1131-127A>G rs10509296
NM_032578.3(MYPN):c.1131-220G>C rs79044605
NM_032578.3(MYPN):c.1131-47A>T rs11598744
NM_032578.3(MYPN):c.1246-235C>T rs12242494
NM_032578.3(MYPN):c.1246-284C>T rs2673801
NM_032578.3(MYPN):c.1246-41T>C rs2817759
NM_032578.3(MYPN):c.1317+135T>A rs7080619
NM_032578.3(MYPN):c.1317+31G>A rs7096613
NM_032578.3(MYPN):c.1318-318T>C rs2176104
NM_032578.3(MYPN):c.1318-322C>T rs2176105
NM_032578.3(MYPN):c.1459+206T>C rs77053350
NM_032578.3(MYPN):c.1459+218A>G rs2673795
NM_032578.3(MYPN):c.1460-151T>A rs10823142
NM_032578.3(MYPN):c.1483+224T>A rs2255136
NM_032578.3(MYPN):c.1484-283T>C rs10823147
NM_032578.3(MYPN):c.1484-336C>T rs10823146
NM_032578.3(MYPN):c.1600+214C>T rs2634709
NM_032578.3(MYPN):c.1600+223C>T rs2634710
NM_032578.3(MYPN):c.1973+170C>T rs10997967
NM_032578.3(MYPN):c.1973+171G>T rs7905579
NM_032578.3(MYPN):c.1973+187A>C rs7905259
NM_032578.3(MYPN):c.1973+264G>A rs45594441
NM_032578.3(MYPN):c.1974-218T>G rs61854651
NM_032578.3(MYPN):c.1974-218_1974-217insG rs199579338
NM_032578.3(MYPN):c.1974-219G>T rs117144583
NM_032578.3(MYPN):c.2564+122G>A rs7917519
NM_032578.3(MYPN):c.2564+203G>T rs10997976
NM_032578.3(MYPN):c.2564+54A>G rs3814183
NM_032578.3(MYPN):c.2565-182A>T rs11330485
NM_032578.3(MYPN):c.2703+178G>T rs10823149
NM_032578.3(MYPN):c.2704-336T>C rs16925246
NM_032578.3(MYPN):c.2925+174T>G rs61857180
NM_032578.3(MYPN):c.2926-178G>A rs1900012
NM_032578.3(MYPN):c.2926-191A>G rs1900013
NM_032578.3(MYPN):c.2926-303T>C rs7094885
NM_032578.3(MYPN):c.3075+182A>G rs7081017
NM_032578.3(MYPN):c.3075+21G>A rs7081213
NM_032578.3(MYPN):c.3075+32C>T rs11815154
NM_032578.3(MYPN):c.3076-67T>A rs7069569
NM_032578.3(MYPN):c.3159-197A>G rs7094660
NM_032578.3(MYPN):c.3159-225G>C rs116829480
NM_032578.3(MYPN):c.3159-261T>C rs6480311
NM_032578.3(MYPN):c.3285+105G>A rs7095603
NM_032578.3(MYPN):c.3285+115G>A rs7095607
NM_032578.3(MYPN):c.3285+140C>T rs7095492
NM_032578.3(MYPN):c.3285+319C>T rs7095774
NM_032578.3(MYPN):c.3286-150G>T rs7079385
NM_032578.3(MYPN):c.3286-192C>A rs12773106
NM_032578.3(MYPN):c.3286-28G>T rs7079549
NM_032578.3(MYPN):c.3493+128T>C rs12358413
NM_032578.3(MYPN):c.3493+235C>A rs10998014
NM_032578.3(MYPN):c.3493+292A>G rs10998015
NM_032578.3(MYPN):c.3493+65G>A rs7079974
NM_032578.3(MYPN):c.3494-116A>G rs7913133
NM_032578.3(MYPN):c.3494-178C>T rs2490937
NM_032578.3(MYPN):c.3494-181A>G rs2490936
NM_032578.3(MYPN):c.3494-218T>G rs2440844
NM_032578.3(MYPN):c.3494-219A>T rs2490935
NM_032578.3(MYPN):c.3494-232A>G rs56008433
NM_032578.3(MYPN):c.3494-233del rs57872028
NM_032578.3(MYPN):c.3494-316C>T rs2490934
NM_032578.3(MYPN):c.3494-85A>G rs7913146
NM_032578.3(MYPN):c.3659+113T>G rs56006628
NM_032578.3(MYPN):c.3659+268C>T rs114853476
NM_032578.3(MYPN):c.3659+311T>C rs10998017
NM_032578.3(MYPN):c.3659+87G>A rs71541554
NM_032578.3(MYPN):c.3660-135T>G rs3814185
NM_032578.3(MYPN):c.3660-276G>A rs3814184
NM_032578.3(MYPN):c.3793+241G>C rs10823157
NM_032578.3(MYPN):c.3794-57C>T rs10998022
NM_032578.3(MYPN):c.903-102T>C rs116204043
NM_032578.3(MYPN):c.903-148T>C rs3814180
NM_032578.3(MYPN):c.903-6294C>T rs116342006
NM_032578.3(MYPN):c.903-6361G>A rs12221035
NM_032578.4(MYPN):c.3481C>A (p.Leu1161Ile) rs138313730

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