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: 14
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HGVS dbSNP
NM_030957.3(ADAMTS10):c.3043-12_3043-6dup rs138501563
NM_030957.4(ADAMTS10):c.*171G>A
NM_030957.4(ADAMTS10):c.*238dup rs151216219
NM_030957.4(ADAMTS10):c.-198A>G
NM_030957.4(ADAMTS10):c.1367G>A (p.Arg456Gln) rs199769798
NM_030957.4(ADAMTS10):c.1588-11C>T
NM_030957.4(ADAMTS10):c.1798-6C>T rs186791828
NM_030957.4(ADAMTS10):c.2016C>T (p.Cys672=) rs10414102
NM_030957.4(ADAMTS10):c.2154G>A (p.Gly718=) rs112185875
NM_030957.4(ADAMTS10):c.2157C>G (p.Ala719=) rs150468696
NM_030957.4(ADAMTS10):c.217G>A (p.Glu73Lys) rs61750006
NM_030957.4(ADAMTS10):c.2261C>T (p.Ser754Phe) rs142353301
NM_030957.4(ADAMTS10):c.2403+4A>G rs187565033
NM_030957.4(ADAMTS10):c.2423T>G (p.Leu808Arg) rs10420313

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