ClinVar Miner

List of variants in gene TRAPPC2 reported as benign for bone disorder

Included ClinVar conditions (1346):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_001011658.4(TRAPPC2):c.*1739C>G rs7716 0.70553
NM_001011658.4(TRAPPC2):c.*830G>C rs1964206 0.65101
NM_001011658.4(TRAPPC2):c.*1052T>C rs5979952 0.28849
NM_001011658.4(TRAPPC2):c.*1599T>C rs146362855 0.01547
NM_001011658.4(TRAPPC2):c.*490C>T rs186451206 0.01542
NM_001011658.4(TRAPPC2):c.*1963A>G rs147081718 0.01377
NM_001011658.4(TRAPPC2):c.*1443G>A rs148298471 0.00704
NM_001011658.4(TRAPPC2):c.*1128C>T rs181174972 0.00702
NM_001011658.4(TRAPPC2):c.*393G>C rs748998980 0.00336
NM_001011658.4(TRAPPC2):c.*394T>C rs780042144 0.00274
NM_001011658.4(TRAPPC2):c.*709C>G rs181594125 0.00235
NM_001011658.4(TRAPPC2):c.*641G>A rs752947538 0.00203
NM_001011658.4(TRAPPC2):c.*2035C>T rs41297317 0.00102
NM_001011658.4(TRAPPC2):c.*546G>A rs777240291 0.00035
NM_001011658.4(TRAPPC2):c.*302A>G rs771210112 0.00009
NM_001011658.4(TRAPPC2):c.*1634G>T rs187464655 0.00001
NM_001011658.4(TRAPPC2):c.*1303del rs35590746
NM_001011658.4(TRAPPC2):c.*1436C>G rs192328990
NM_001011658.4(TRAPPC2):c.*2104TG[4] rs199924403
NM_001011658.4(TRAPPC2):c.*956_*957insTTTTTTTT rs57103709

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