ClinVar Miner

List of variants reported as uncertain significance for Congenital generalized lipodystrophy type 1

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Total variants: 52
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HGVS dbSNP
NM_006412.4(AGPAT2):c.*164C>A rs777619886
NM_006412.4(AGPAT2):c.*201G>C rs567964604
NM_006412.4(AGPAT2):c.*211G>A
NM_006412.4(AGPAT2):c.*217G>A rs886063720
NM_006412.4(AGPAT2):c.*232C>T
NM_006412.4(AGPAT2):c.*277C>T
NM_006412.4(AGPAT2):c.*34C>G
NM_006412.4(AGPAT2):c.*354C>T rs886063719
NM_006412.4(AGPAT2):c.*382C>T
NM_006412.4(AGPAT2):c.*411C>T
NM_006412.4(AGPAT2):c.*418G>A rs886063718
NM_006412.4(AGPAT2):c.*45C>A rs769602973
NM_006412.4(AGPAT2):c.*488C>T
NM_006412.4(AGPAT2):c.*512G>A rs555467686
NM_006412.4(AGPAT2):c.*514A>C rs886063717
NM_006412.4(AGPAT2):c.*572C>T
NM_006412.4(AGPAT2):c.-18C>A
NM_006412.4(AGPAT2):c.-19T>C
NM_006412.4(AGPAT2):c.-4G>C rs886063724
NM_006412.4(AGPAT2):c.-61G>C rs886063725
NM_006412.4(AGPAT2):c.-62G>A rs566958496
NM_006412.4(AGPAT2):c.-68C>G rs886063726
NM_006412.4(AGPAT2):c.199G>A (p.Val67Met) rs563539429
NM_006412.4(AGPAT2):c.234C>T (p.Phe78=) rs543374987
NM_006412.4(AGPAT2):c.269G>A (p.Arg90His) rs142176861
NM_006412.4(AGPAT2):c.282C>T (p.Ile94=)
NM_006412.4(AGPAT2):c.315G>T (p.Met105Ile) rs746809573
NM_006412.4(AGPAT2):c.316+15G>A rs531012485
NM_006412.4(AGPAT2):c.335C>T (p.Pro112Leu) rs886063722
NM_006412.4(AGPAT2):c.361C>G (p.Arg121Gly)
NM_006412.4(AGPAT2):c.397A>G (p.Met133Val)
NM_006412.4(AGPAT2):c.415T>G (p.Phe139Val)
NM_006412.4(AGPAT2):c.453A>G (p.Thr151=) rs886063721
NM_006412.4(AGPAT2):c.476G>T (p.Arg159Leu) rs374919945
NM_006412.4(AGPAT2):c.483C>T (p.Val161=) rs370441324
NM_006412.4(AGPAT2):c.492+4_492+7del rs1057518715
NM_006412.4(AGPAT2):c.493-7C>T
NM_006412.4(AGPAT2):c.54G>A (p.Val18=)
NM_006412.4(AGPAT2):c.604G>A (p.Val202Met) rs372408400
NM_006412.4(AGPAT2):c.646A>T (p.Lys216Ter) rs138994150
NM_006412.4(AGPAT2):c.647A>T (p.Lys216Met)
NM_006412.4(AGPAT2):c.698C>A (p.Thr233Asn) rs536777709
NM_006412.4(AGPAT2):c.720C>T (p.Asp240=) rs142207711
NM_006412.4(AGPAT2):c.732C>T (p.Leu244=) rs200288462
NM_006412.4(AGPAT2):c.748C>T (p.Arg250Trp) rs767338891
NM_006412.4(AGPAT2):c.749G>A (p.Arg250Gln)
NM_006412.4(AGPAT2):c.762C>T (p.Thr254=) rs146973799
NM_006412.4(AGPAT2):c.783G>A (p.Lys261=) rs761143874
NM_006412.4(AGPAT2):c.786C>T (p.Thr262=)
NM_006412.4(AGPAT2):c.788C>T (p.Pro263Leu)
NM_006412.4(AGPAT2):c.813G>T (p.Gly271=)
NM_006412.4(AGPAT2):c.820G>A (p.Val274Met) rs368902934

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