ClinVar Miner

List of variants in gene ADAMTS2 reported as likely benign by Invitae

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Gene type:
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Total variants: 19
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HGVS dbSNP
NM_014244.4(ADAMTS2):c.1149C>T (p.Thr383=) rs199664723
NM_014244.4(ADAMTS2):c.1254C>T (p.His418=) rs758041605
NM_014244.4(ADAMTS2):c.1431G>A (p.Ala477=) rs147259971
NM_014244.4(ADAMTS2):c.2034G>A (p.Thr678=) rs139943837
NM_014244.4(ADAMTS2):c.2267T>C (p.Val756Ala) rs141650732
NM_014244.4(ADAMTS2):c.2292C>T (p.Ala764=) rs188566209
NM_014244.4(ADAMTS2):c.2466G>T (p.Pro822=) rs377085746
NM_014244.4(ADAMTS2):c.2469G>A (p.Val823=) rs182103023
NM_014244.4(ADAMTS2):c.2750+10C>T rs1045751866
NM_014244.4(ADAMTS2):c.2795G>A (p.Arg932Gln) rs140022033
NM_014244.4(ADAMTS2):c.2817C>T (p.Ser939=) rs201215425
NM_014244.4(ADAMTS2):c.2892C>T (p.Pro964=) rs546361762
NM_014244.4(ADAMTS2):c.2893G>A (p.Glu965Lys) rs144138766
NM_014244.4(ADAMTS2):c.2994G>T (p.Arg998=) rs780314895
NM_014244.4(ADAMTS2):c.3078C>A (p.Gly1026=) rs886060491
NM_014244.4(ADAMTS2):c.3342C>T (p.Asn1114=) rs79606317
NM_014244.4(ADAMTS2):c.580T>C (p.Leu194=) rs1554094148
NM_014244.4(ADAMTS2):c.732C>T (p.Gly244=) rs143069972
NM_014244.4(ADAMTS2):c.748G>A (p.Ala250Thr) rs143764421

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