List of variants in gene TRAPPC2 reported as benign for Spondyloepiphyseal dysplasia tarda

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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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	0.00100
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	0.00004
NM_001011658.4(TRAPPC2):c.*1436C>G	rs192328990

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