ClinVar Miner

List of variants in gene COMP 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: 21
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HGVS dbSNP gnomAD frequency
NM_000095.3(COMP):c.2267A>G (p.Gln756Arg) rs61752496 0.06295
NM_000095.3(COMP):c.*1G>C rs77185131 0.06291
NM_000095.3(COMP):c.1755G>A (p.Thr585=) rs34467947 0.04927
NM_000095.3(COMP):c.1156A>G (p.Asn386Asp) rs61739916 0.03133
NM_000095.3(COMP):c.511G>A (p.Ala171Thr) rs115338183 0.01840
NM_000095.3(COMP):c.1956C>T (p.Asn652=) rs10421797 0.00834
NM_000095.3(COMP):c.762+12C>A rs199733531 0.00463
NM_000095.3(COMP):c.*92G>A rs9407 0.00384
NM_000095.3(COMP):c.2227+8G>A rs116499541 0.00363
NM_000095.3(COMP):c.218-15C>A rs542886784 0.00199
NM_000095.3(COMP):c.*15A>G rs201937857 0.00126
NM_000095.3(COMP):c.-9G>T rs186562511 0.00123
NM_000095.3(COMP):c.279C>A (p.Pro93=) rs139319996 0.00093
NM_000095.3(COMP):c.2152C>A (p.Arg718=) rs28936368 0.00081
NM_000095.3(COMP):c.468G>T (p.Pro156=) rs202241721 0.00017
NM_000095.3(COMP):c.924C>T (p.Ile308=) rs199596155 0.00007
NM_000095.3(COMP):c.1668+13T>A rs74432818
NM_000095.3(COMP):c.1668+13T>G rs74432818
NM_000095.3(COMP):c.195G>A (p.Thr65=) rs529891904
NM_000095.3(COMP):c.218-14C>T rs150008764
NM_000095.3(COMP):c.218-6C>G rs534407430

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