ClinVar Miner

List of variants in gene TREM2 studied for autosomal recessive disease

Included ClinVar conditions (1198):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 45
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HGVS dbSNP gnomAD frequency
NM_018965.4(TREM2):c.632T>C (p.Leu211Pro) rs2234256 0.04010
NM_018965.4(TREM2):c.*73G>A rs2234258 0.01125
NM_018965.4(TREM2):c.185G>A (p.Arg62His) rs143332484 0.00714
NM_018965.4(TREM2):c.469C>T (p.His157Tyr) rs2234255 0.00187
NM_018965.4(TREM2):c.140G>A (p.Arg47His) rs75932628 0.00153
NM_018965.4(TREM2):c.259G>A (p.Asp87Asn) rs142232675 0.00152
NM_018965.4(TREM2):c.399G>T (p.Leu133=) rs144250872 0.00095
NM_018965.4(TREM2):c.451G>A (p.Glu151Lys) rs79011726 0.00026
NM_018965.4(TREM2):c.668C>T (p.Thr223Ile) rs138355759 0.00026
NM_018965.4(TREM2):c.40+13C>T rs145658858 0.00016
NM_018965.4(TREM2):c.690G>A (p.Thr230=) rs199795809 0.00015
NM_018965.4(TREM2):c.*48A>T rs200820365 0.00014
NM_018965.3(TREM2):c.-98C>T rs558304800 0.00011
NM_018965.4(TREM2):c.393C>T (p.Asp131=) rs139607688 0.00010
NM_018965.4(TREM2):c.574G>A (p.Ala192Thr) rs150277350 0.00010
NM_018965.4(TREM2):c.*30G>A rs75272959 0.00009
NM_018965.4(TREM2):c.*156G>T rs768583708 0.00007
NM_018965.4(TREM2):c.*148C>T rs761884997 0.00005
NM_018965.4(TREM2):c.117C>G (p.Asp39Glu) rs200392967 0.00005
NM_018965.4(TREM2):c.486C>G (p.Ser162Arg) rs371702633 0.00005
NM_018965.4(TREM2):c.197C>T (p.Thr66Met) rs201258663 0.00004
NM_018965.4(TREM2):c.514C>T (p.Pro172Ser) rs781302866 0.00003
NM_018965.4(TREM2):c.97C>T (p.Gln33Ter) rs104894002 0.00002
NM_018965.3(TREM2):c.-51G>A rs3747741 0.00001
NM_018965.4(TREM2):c.*111A>G rs753777378 0.00001
NM_018965.4(TREM2):c.*157G>A rs1232354245 0.00001
NM_018965.4(TREM2):c.115G>A (p.Asp39Asn) rs764816591 0.00001
NM_018965.4(TREM2):c.132G>A (p.Trp44Ter) rs104894001 0.00001
NM_018965.4(TREM2):c.233G>A (p.Trp78Ter) rs104893998 0.00001
NM_018965.4(TREM2):c.313del (p.Ala105fs) rs386834141 0.00001
NM_018965.4(TREM2):c.377T>G (p.Val126Gly) rs121908402 0.00001
NM_018965.4(TREM2):c.482+2T>C rs386834144 0.00001
NM_018965.4(TREM2):c.482+7C>T rs746496916 0.00001
NM_018965.4(TREM2):c.113A>G (p.Tyr38Cys) rs797044603
NM_018965.4(TREM2):c.203A>T (p.Asn68Ile)
NM_018965.4(TREM2):c.254C>T (p.Thr85Ile) rs368255898
NM_018965.4(TREM2):c.269del (p.Gly90fs) rs386834140
NM_018965.4(TREM2):c.287C>A (p.Thr96Lys) rs2234253
NM_018965.4(TREM2):c.292C>T (p.Arg98Trp) rs147564421
NM_018965.4(TREM2):c.346A>T (p.Ser116Cys) rs2113879950
NM_018965.4(TREM2):c.40+1G>A
NM_018965.4(TREM2):c.40+4_40+6del rs386834142
NM_018965.4(TREM2):c.401A>G (p.Asp134Gly) rs28939079
NM_018965.4(TREM2):c.40G>T (p.Glu14Ter) rs386834143
NM_018965.4(TREM2):c.558G>T (p.Lys186Asn) rs28937876

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