ClinVar Miner

List of variants in gene APP reported as benign for Alzheimer disease

Included ClinVar conditions (17):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
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HGVS dbSNP
NM_000484.4(APP):c.*724C>T
NM_000484.4(APP):c.*913C>G rs202081585
NM_000484.4(APP):c.*914G>A rs736479
NM_000484.4(APP):c.*967G>A rs45541739
NM_000484.4(APP):c.-111G>C rs459543
NM_000484.4(APP):c.1299+9T>C rs114675472
NM_000484.4(APP):c.1305C>T (p.Phe435=) rs148180403
NM_000484.4(APP):c.1614T>C (p.Tyr538=) rs45537238
NM_000484.4(APP):c.1795G>A (p.Glu599Lys) rs140304729
NM_000484.4(APP):c.1840A>G (p.Ser614Gly) rs112263157
NM_000484.4(APP):c.2124C>T (p.Gly708=) rs148888161
NM_000484.4(APP):c.2133C>A (p.Val711=) rs116650065
NM_000484.4(APP):c.2148C>A (p.Ile716=) rs145564988
NM_000484.4(APP):c.2212-10T>C rs45513597
NM_000484.4(APP):c.2212-11_2212-10del rs112965435
NM_000484.4(APP):c.2217C>T (p.Asp739=) rs145277462
NM_000484.4(APP):c.225+7C>A rs201865168
NM_000484.4(APP):c.592T>C (p.Ser198Pro) rs145081708
NM_000484.4(APP):c.663-9C>A rs199587668
NM_000484.4(APP):c.741C>T (p.Asp247=) rs148832151
NM_000484.4(APP):c.826A>T (p.Thr276Ser) rs202198008
NM_000484.4(APP):c.975C>T (p.Gly325=) rs201622977

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