ClinVar Miner

List of variants in gene MYLK2 reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 61
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_033118.4(MYLK2):c.973-141G>T rs11907637 0.01341
NM_033118.4(MYLK2):c.879-262C>T rs115124478 0.01267
NM_033118.4(MYLK2):c.1711-182G>A rs114661585 0.01253
NM_033118.4(MYLK2):c.772+84G>A rs114835664 0.00721
NM_033118.4(MYLK2):c.773-173T>C rs142431797 0.00476
NM_033118.4(MYLK2):c.972+67G>A rs8116429 0.00435
NM_033118.4(MYLK2):c.508G>A (p.Glu170Lys) rs145656924 0.00175
NM_033118.4(MYLK2):c.4G>A (p.Ala2Thr) rs117502839 0.00141
NM_033118.4(MYLK2):c.53-45A>G rs2182966 0.00074
NM_033118.4(MYLK2):c.524C>A (p.Thr175Asn) rs202084078 0.00066
NM_033118.4(MYLK2):c.878+95C>A rs115953332 0.00055
NM_033118.4(MYLK2):c.1778C>T (p.Ala593Val) rs146497334 0.00051
NM_033118.4(MYLK2):c.834T>A (p.Asn278Lys) rs41293104 0.00044
NM_033118.4(MYLK2):c.783G>A (p.Pro261=) rs144621796 0.00036
NM_033118.4(MYLK2):c.786A>G (p.Pro262=) rs727504437 0.00029
NM_033118.4(MYLK2):c.1176C>T (p.Asp392=) rs147099889 0.00027
NM_033118.4(MYLK2):c.473+11C>T rs373880854 0.00027
NM_033118.4(MYLK2):c.*9C>T rs199816743 0.00020
NM_033118.4(MYLK2):c.157G>A (p.Asp53Asn) rs200204126 0.00017
NM_033118.4(MYLK2):c.726G>A (p.Gln242=) rs145772898 0.00017
NM_033118.4(MYLK2):c.260C>T (p.Ala87Val) rs121908107 0.00014
NM_033118.4(MYLK2):c.50C>A (p.Thr17Lys) rs192056427 0.00013
NM_033118.4(MYLK2):c.281C>T (p.Pro94Leu) rs201134349 0.00012
NM_033118.4(MYLK2):c.828C>T (p.Thr276=) rs370429139 0.00011
NM_033118.4(MYLK2):c.1590C>T (p.Asn530=) rs374233822 0.00010
NM_033118.4(MYLK2):c.1225-20G>T rs368839195 0.00009
NM_033118.4(MYLK2):c.261G>A (p.Ala87=) rs374353729 0.00009
NM_033118.4(MYLK2):c.1224+8A>C rs375144075 0.00006
NM_033118.4(MYLK2):c.331C>T (p.Pro111Ser) rs750548324 0.00006
NM_033118.4(MYLK2):c.595A>G (p.Ile199Val) rs193922712 0.00006
NM_033118.4(MYLK2):c.1123G>A (p.Asp375Asn) rs397517472 0.00005
NM_033118.4(MYLK2):c.1710+5C>T rs574644297 0.00005
NM_033118.4(MYLK2):c.1401T>C (p.Ser467=) rs770625966 0.00004
NM_033118.4(MYLK2):c.1248C>T (p.Asn416=) rs138459623 0.00003
NM_033118.4(MYLK2):c.1082+10C>T rs770363702 0.00002
NM_033118.4(MYLK2):c.1424+20G>A rs375290219 0.00002
NM_033118.4(MYLK2):c.1431C>T (p.Ser477=) rs764056444 0.00002
NM_033118.4(MYLK2):c.258C>T (p.Pro86=) rs149280577 0.00002
NM_033118.4(MYLK2):c.933G>C (p.Leu311=) rs146745888 0.00002
NM_033118.4(MYLK2):c.*1G>T rs749491327 0.00001
NM_033118.4(MYLK2):c.1092C>T (p.Gly364=) rs745574239 0.00001
NM_033118.4(MYLK2):c.1137C>T (p.Thr379=) rs759608229 0.00001
NM_033118.4(MYLK2):c.1233C>T (p.Asn411=) rs200963586 0.00001
NM_033118.4(MYLK2):c.1577+9C>T rs373252847 0.00001
NM_033118.4(MYLK2):c.1764G>A (p.Ser588=) rs758879929 0.00001
NM_033118.4(MYLK2):c.249C>T (p.Gly83=) rs774383057 0.00001
NM_033118.4(MYLK2):c.294C>T (p.Pro98=) rs373609417 0.00001
NM_033118.4(MYLK2):c.310C>T (p.Pro104Ser) rs794729066 0.00001
NM_033118.4(MYLK2):c.471C>T (p.Ser157=) rs1033301935 0.00001
NM_033118.4(MYLK2):c.609C>T (p.Ser203=) rs748858933 0.00001
NM_033118.4(MYLK2):c.879-13C>T rs367859025 0.00001
NM_033118.4(MYLK2):c.972+13C>T rs876657524 0.00001
NC_000020.11:g.31819321del rs556265822
NM_033118.4(MYLK2):c.*27G>T rs181337772
NM_033118.4(MYLK2):c.-62C>T rs1555789794
NM_033118.4(MYLK2):c.1224+201del rs201098253
NM_033118.4(MYLK2):c.1296-13G>T rs759181721
NM_033118.4(MYLK2):c.420G>A (p.Arg140=) rs1555789909
NM_033118.4(MYLK2):c.473+10C>T rs958044110
NM_033118.4(MYLK2):c.878+8C>G rs1057521284
NM_033118.4(MYLK2):c.879-7T>C rs1057521613

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.