List of variants reported as not provided for laminopathy

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		ClinVar version:

Total variants: 33

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HGVS	dbSNP	gnomAD frequency
NM_182914.3(SYNE2):c.19135C>T (p.Arg6379Cys)	rs141741640	0.00138
NM_182961.4(SYNE1):c.11218A>G (p.Thr3740Ala)	rs144797744	0.00034
NM_182961.4(SYNE1):c.20737C>T (p.Arg6913Cys)	rs142593312	0.00011
NM_182914.3(SYNE2):c.20039G>A (p.Arg6680Gln)	rs761684738	0.00003
NM_001159699.2(FHL1):c.812G>C (p.Cys271Ser)	rs869025431	0.00001
NM_170707.4(LMNA):c.1045C>T (p.Arg349Trp)	rs267607555	0.00001
NM_170707.4(LMNA):c.1303C>T (p.Arg435Cys)	rs150840924	0.00001
NM_170707.4(LMNA):c.1579C>T (p.Arg527Cys)	rs57318642	0.00001
NM_170707.4(LMNA):c.1380+1G>A	rs267607552
NM_170707.4(LMNA):c.1564T>C (p.Cys522Arg)	rs1572366516
NM_170707.4(LMNA):c.1619T>C (p.Met540Thr)	rs267607547
NM_170707.4(LMNA):c.16C>T (p.Gln6Ter)	rs61046466
NM_170707.4(LMNA):c.1700_1968+1del	rs1553266460
NM_170707.4(LMNA):c.1771T>A (p.Cys591Ser)	rs797044486
NM_170707.4(LMNA):c.1821G>A (p.Val607=)	rs59886214
NM_170707.4(LMNA):c.1822G>A (p.Gly608Ser)	rs61064130
NM_170707.4(LMNA):c.1824C>T (p.Gly608=)	rs58596362
NM_170707.4(LMNA):c.1868C>G (p.Thr623Ser)	rs59267781
NM_170707.4(LMNA):c.1968+1G>A	rs113436208
NM_170707.4(LMNA):c.1968+1G>C	rs113436208
NM_170707.4(LMNA):c.1968+2T>A	rs113860699
NM_170707.4(LMNA):c.1968+2T>C	rs113860699
NM_170707.4(LMNA):c.1968+5G>A	rs797044488
NM_170707.4(LMNA):c.1968+5G>C	rs797044488
NM_170707.4(LMNA):c.1968G>A (p.Gln656=)	rs797044487
NM_170707.4(LMNA):c.433G>A (p.Glu145Lys)	rs60310264
NM_170707.4(LMNA):c.607G>A (p.Glu203Lys)	rs61195471
NM_170707.4(LMNA):c.664C>T (p.His222Tyr)	rs28928901
NM_170707.4(LMNA):c.667G>A (p.Glu223Lys)	rs797044485
NM_170707.4(LMNA):c.674G>A (p.Arg225Gln)	rs199474724
NM_170707.4(LMNA):c.694G>C (p.Gly232Arg)	rs267607609
NM_182914.3(SYNE2):c.13693C>G (p.Gln4565Glu)	rs2153672399
NM_182914.3(SYNE2):c.15527A>T (p.Glu5176Val)	rs1595828652

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