ClinVar Miner

List of variants in gene COMP reported as likely benign for bone disorder

Included ClinVar conditions (1346):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
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HGVS dbSNP gnomAD frequency
NM_000095.3(COMP):c.218-15C>A rs542886784 0.00199
NM_000095.2(COMP):c.*155G>C rs537572167 0.00130
NM_000095.3(COMP):c.-9G>T rs186562511 0.00123
NM_000095.3(COMP):c.360C>T (p.Gly120=) rs150820366 0.00044
NM_000095.3(COMP):c.868-4C>T rs529806631 0.00019
NM_000095.3(COMP):c.410T>C (p.Phe137Ser) rs757094319 0.00017
NM_000095.3(COMP):c.2213G>A (p.Arg738His) rs766913050 0.00009
NM_000095.3(COMP):c.1979C>G (p.Thr660Arg) rs150534218 0.00007
NM_000095.3(COMP):c.924C>T (p.Ile308=) rs199596155 0.00007
NM_000095.3(COMP):c.1200C>T (p.Gly400=) rs201063220 0.00003
NM_000095.3(COMP):c.588G>A (p.Val196=) rs201165293 0.00001
NM_000095.3(COMP):c.218-6C>G rs534407430

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