List of variants reported as uncertain significance for chromosome 7 disorder by Fulgent Genetics, Fulgent Genetics

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Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_000501.4(ELN):c.1358-199G>A	rs781963901	0.00034
NM_000501.4(ELN):c.647G>T (p.Gly216Val)	rs145612009	0.00034
NM_000501.4(ELN):c.1373C>A (p.Ala458Glu)	rs149117932	0.00021
NM_000501.4(ELN):c.1675G>A (p.Val559Ile)	rs560081099	0.00015
NM_000501.4(ELN):c.35G>T (p.Gly12Val)	rs367634266	0.00012
NM_000501.4(ELN):c.202G>A (p.Gly68Arg)	rs372566075	0.00011
NM_000501.4(ELN):c.403G>A (p.Gly135Arg)	rs373650953	0.00007
NM_000501.4(ELN):c.1543G>A (p.Val515Met)	rs376258672	0.00006
NM_000501.4(ELN):c.1943G>A (p.Gly648Glu)	rs140085632	0.00003
NM_000501.4(ELN):c.1150G>A (p.Gly384Arg)	rs782359367	0.00001
NM_000501.3(ELN):c.-70G>C	rs537200597
NM_000501.4(ELN):c.1591_1592delinsTT (p.Ala531Phe)	rs863223529

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