List of variants in gene MYLK2 reported as benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 39

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HGVS	dbSNP	gnomAD frequency
NM_033118.4(MYLK2):c.473+231T>C	rs4911532	0.68245
NM_033118.4(MYLK2):c.1711-296T>G	rs6087783	0.42378
NM_033118.4(MYLK2):c.1224+201G>A	rs6060976	0.41753
NM_033118.4(MYLK2):c.1711-61C>T	rs6089093	0.29286
NM_033118.4(MYLK2):c.1424+107A>G	rs4518038	0.16250
NM_033118.4(MYLK2):c.1710+15A>G	rs6060980	0.09349
NM_033118.4(MYLK2):c.473+86T>C	rs12480305	0.09221
NM_033118.4(MYLK2):c.878+42T>C	rs6060971	0.09170
NM_033118.4(MYLK2):c.684T>C (p.Ile228=)	rs6058469	0.09162
NM_033118.4(MYLK2):c.1083-40C>G	rs41293108	0.09160
NM_033118.4(MYLK2):c.878+215C>T	rs6060972	0.09159
NM_033118.4(MYLK2):c.879-240C>T	rs6060973	0.09158
NM_033118.4(MYLK2):c.53-230G>A	rs1009454	0.09138
NM_033118.4(MYLK2):c.973-74G>A	rs11907651	0.09124
NM_033118.4(MYLK2):c.772+33C>T	rs6060970	0.08970
NM_033118.4(MYLK2):c.1710+245A>G	rs6058471	0.08957
NM_033118.4(MYLK2):c.1710+120C>T	rs28763881	0.08956
NM_033118.4(MYLK2):c.-67T>C	rs1887731	0.08100
NM_033118.4(MYLK2):c.1082+11G>A	rs76530988	0.01993
NM_033118.4(MYLK2):c.1104C>T (p.Phe368=)	rs6089088	0.01807
NM_033118.4(MYLK2):c.266G>A (p.Gly89Asp)	rs115398036	0.01365
NM_033118.4(MYLK2):c.430C>G (p.Pro144Ala)	rs34396614	0.01268
NM_033118.4(MYLK2):c.1068C>T (p.Val356=)	rs17340492	0.01201
NM_033118.4(MYLK2):c.918C>T (p.Ala306=)	rs41293106	0.01179
NM_033118.4(MYLK2):c.1711-6C>T	rs76603530	0.00376
NM_033118.4(MYLK2):c.1711-20C>G	rs189282373	0.00374
NM_033118.4(MYLK2):c.284C>A (p.Ala95Glu)	rs121908108	0.00202
NM_033118.4(MYLK2):c.1458T>C (p.Asp486=)	rs111888319	0.00180
NM_033118.4(MYLK2):c.1295+4C>A	rs113936360	0.00179
NM_033118.4(MYLK2):c.791C>T (p.Pro264Leu)	rs142620954	0.00165
NM_033118.4(MYLK2):c.1584G>A (p.Arg528=)	rs55807353	0.00120
NM_033118.4(MYLK2):c.102A>G (p.Lys34=)	rs28763880	0.00101
NM_033118.4(MYLK2):c.173C>A (p.Ala58Asp)	rs138130914	0.00070
NM_033118.4(MYLK2):c.549C>T (p.His183=)	rs3746597	0.00035
NM_033118.4(MYLK2):c.1308C>T (p.Asn436=)	rs369603764	0.00023
NM_033118.4(MYLK2):c.972+14G>A	rs193922713	0.00020
NM_033118.4(MYLK2):c.6G>A (p.Ala2=)	rs201983158	0.00003
NM_033118.4(MYLK2):c.627G>A (p.Glu209=)	rs587781091
NM_033118.4(MYLK2):c.772+44G>C	rs35574032

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