ClinVar Miner

List of variants in gene ADAMTS10 reported as likely benign for Weill-Marchesani syndrome

Included ClinVar conditions (8):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 13
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HGVS dbSNP
NM_030957.3(ADAMTS10):c.3043-12_3043-6dup rs138501563
NM_030957.4(ADAMTS10):c.*238dup rs151216219
NM_030957.4(ADAMTS10):c.*428A>G rs116024095
NM_030957.4(ADAMTS10):c.1350G>T (p.Gly450=) rs75734496
NM_030957.4(ADAMTS10):c.1588-7C>G rs11882422
NM_030957.4(ADAMTS10):c.1803T>C (p.Cys601=) rs115093676
NM_030957.4(ADAMTS10):c.185G>A (p.Arg62Gln) rs62621197
NM_030957.4(ADAMTS10):c.1900+11G>C rs78421590
NM_030957.4(ADAMTS10):c.1901-11G>A rs117220199
NM_030957.4(ADAMTS10):c.2423T>G (p.Leu808Arg) rs10420313
NM_030957.4(ADAMTS10):c.2584G>T (p.Ala862Ser) rs10418929
NM_030957.4(ADAMTS10):c.3102G>A (p.Thr1034=) rs10405956
NM_030957.4(ADAMTS10):c.356G>A (p.Arg119Gln) rs3814291

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