ClinVar Miner

List of variants in gene MECP2 reported as uncertain significance for Autism, susceptibility to, X-linked 3

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Total variants: 23
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HGVS dbSNP
NM_004992.3(MECP2):c.*1368C>A rs267608355
NM_004992.3(MECP2):c.*177G>C rs267608345
NM_004992.3(MECP2):c.*204G>A rs267608352
NM_004992.3(MECP2):c.*2556T>A rs267608356
NM_004992.3(MECP2):c.*2657G>A rs3027921
NM_004992.3(MECP2):c.*2706G>A rs267608357
NM_004992.3(MECP2):c.*2956G>A rs267608358
NM_004992.3(MECP2):c.*3658C>T rs267608359
NM_004992.3(MECP2):c.*371G>C rs187851059
NM_004992.3(MECP2):c.*5348T>C rs267608346
NM_004992.3(MECP2):c.*544G>A rs183349022
NM_004992.3(MECP2):c.*554G>A rs267608353
NM_004992.3(MECP2):c.*767G>T rs267608354
NM_004992.3(MECP2):c.*861T>G rs187614438
NM_004992.3(MECP2):c.1127C>G (p.Pro376Arg) rs61752976
NM_004992.3(MECP2):c.27-55G>A rs267608414
NM_004992.3(MECP2):c.377+18C>G rs267608461
NM_004992.3(MECP2):c.377+6_377+9delTAAG rs267608459
NM_004992.3(MECP2):c.479C>G (p.Thr160Ser) rs61748414
NM_004992.3(MECP2):c.542C>T (p.Ala181Val) rs61749705
NM_004992.3(MECP2):c.617G>C (p.Gly206Ala) rs63485860
NM_004992.3(MECP2):c.898G>A (p.Val300Ile) rs61751370
NM_004992.3(MECP2):c.925C>T (p.Arg309Trp) rs61751444

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