ClinVar Miner

List of variants in gene CDH1 reported as likely benign by Preventiongenetics, part of Exact Sciences

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Gene type:
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Total variants: 23
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HGVS dbSNP gnomAD frequency
NM_004360.5(CDH1):c.532-18C>T rs200673941 0.00398
NM_004360.5(CDH1):c.2292C>T (p.Asp764=) rs61747636 0.00159
NM_004360.5(CDH1):c.1272C>T (p.Val424=) rs61756284 0.00143
NM_004360.5(CDH1):c.88C>A (p.Pro30Thr) rs139866691 0.00129
NM_004360.5(CDH1):c.1744C>T (p.Leu582=) rs1801025 0.00045
NM_004360.5(CDH1):c.687+77G>A rs542845447 0.00024
NM_004360.5(CDH1):c.687+33G>A rs199545571 0.00023
NM_004360.5(CDH1):c.33G>C (p.Leu11=) rs730881654 0.00022
NM_004360.5(CDH1):c.1711+9G>A rs368770384 0.00010
NM_004360.5(CDH1):c.1359C>T (p.His453=) rs114861467 0.00009
NM_004360.5(CDH1):c.1422C>T (p.Thr474=) rs375843744 0.00006
NM_004360.5(CDH1):c.393C>T (p.Ser131=) rs145430811 0.00006
NM_004360.5(CDH1):c.1224G>A (p.Ala408=) rs200161607 0.00004
NM_004360.5(CDH1):c.1936+8C>T rs776624068 0.00004
NM_004360.5(CDH1):c.188G>A (p.Arg63Gln) rs587780117 0.00002
NM_004360.5(CDH1):c.388-8C>T rs774601444 0.00002
NM_004360.5(CDH1):c.510A>G (p.Pro170=) rs774962542 0.00002
NM_004360.5(CDH1):c.1833C>T (p.Val611=) rs748413209 0.00001
NM_004360.5(CDH1):c.2358C>T (p.Asp786=) rs760701558 0.00001
NM_004360.5(CDH1):c.286A>G (p.Ile96Val) rs749306433 0.00001
NM_004360.5(CDH1):c.*20C>T rs781160222
NM_004360.5(CDH1):c.-8G>T rs879449703
NM_004360.5(CDH1):c.1356A>G (p.Leu452=) rs61747633

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