ClinVar Miner

List of variants in gene APP reported as uncertain significance for Alzheimer disease

Included ClinVar conditions (13):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 31
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HGVS dbSNP
NM_000484.3(APP):c.*1015T>G rs202108412
NM_000484.3(APP):c.*194A>C rs199977643
NM_000484.3(APP):c.*735G>A rs202132811
NM_000484.3(APP):c.*97C>A rs886056992
NM_000484.3(APP):c.-132G>T rs886056998
NM_000484.3(APP):c.-170C>A rs538664273
NM_000484.3(APP):c.-186G>T rs886056999
NM_000484.3(APP):c.-199G>A rs761755102
NM_000484.3(APP):c.-200G>A rs200621906
NM_000484.3(APP):c.-44C>T rs200289921
NM_000484.3(APP):c.121C>G (p.Leu41Val) rs886056997
NM_000484.3(APP):c.1224+12T>C rs200725014
NM_000484.3(APP):c.126C>T (p.Asn42=) rs745974049
NM_000484.3(APP):c.1380A>G (p.Arg460=) rs745834578
NM_000484.3(APP):c.1458+9C>T rs201937048
NM_000484.3(APP):c.1642C>G (p.Leu548Val) rs886056994
NM_000484.3(APP):c.1664C>T (p.Ala555Val) rs886056993
NM_000484.3(APP):c.1689T>C (p.Asp563=) rs137865262
NM_000484.3(APP):c.1810G>A (p.Val604Met) rs199887707
NM_000484.3(APP):c.2064+10A>T rs202051599
NM_000484.3(APP):c.2137G>A (p.Ala713Thr) rs63750066
NM_000484.3(APP):c.225+14G>A rs199644062
NM_000484.3(APP):c.237A>G (p.Glu79=) rs886056996
NM_000484.3(APP):c.355+6C>T rs1555873548
NM_000484.3(APP):c.355+9G>A rs371324252
NM_000484.3(APP):c.468+11A>G rs886056995
NM_000484.3(APP):c.592T>C (p.Ser198Pro) rs145081708
NM_000484.3(APP):c.602C>T (p.Ala201Val) rs149995579
NM_000484.3(APP):c.618G>A (p.Ser206=) rs201022619
NM_000484.3(APP):c.674T>C (p.Val225Ala) rs746313873
NM_000484.3(APP):c.837_839dupCAC (p.Thr280_Glu281insThr) rs527890624

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