List of variants in gene ADAMTS10 reported as likely benign for acromelic dysplasia

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_030957.4(ADAMTS10):c.2423T>G (p.Leu808Arg)	rs10420313	0.02947
NM_030957.4(ADAMTS10):c.1588-7C>G	rs11882422	0.02550
NM_030957.4(ADAMTS10):c.-198A>G	rs4530289	0.01712
NM_030957.4(ADAMTS10):c.*171G>A	rs79238375	0.00991
NM_030957.4(ADAMTS10):c.2403+4A>G	rs187565033	0.00608
NM_030957.4(ADAMTS10):c.2157C>G (p.Ala719=)	rs150468696	0.00463
NM_030957.4(ADAMTS10):c.2016C>T (p.Cys672=)	rs10414102	0.00419
NM_030957.4(ADAMTS10):c.217G>A (p.Glu73Lys)	rs61750006	0.00419
NM_030957.4(ADAMTS10):c.2154G>A (p.Gly718=)	rs112185875	0.00213
NM_030957.4(ADAMTS10):c.2261C>T (p.Ser754Phe)	rs142353301	0.00203
NM_030957.4(ADAMTS10):c.1588-11C>T	rs112970413	0.00142
NM_030957.4(ADAMTS10):c.1798-6C>T	rs186791828	0.00064
NM_030957.4(ADAMTS10):c.1367G>A (p.Arg456Gln)	rs199769798	0.00012
NM_030957.4(ADAMTS10):c.68C>T (p.Thr23Met)	rs376131325	0.00008
NM_030957.3(ADAMTS10):c.3043-12_3043-6dup	rs138501563
NM_030957.4(ADAMTS10):c.*238dup	rs151216219

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