ClinVar Miner

List of variants in gene CLN6 reported as benign for not provided

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Gene type:
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Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_017882.3(CLN6):c.199-252A>C rs6494721 0.99323
NM_017882.3(CLN6):c.198+104T>C rs8025947 0.57324
NM_017882.3(CLN6):c.83+188T>C rs55954678 0.56414
NM_017882.3(CLN6):c.665+265G>A rs11632516 0.46738
NM_017882.3(CLN6):c.*38A>G rs757788122 0.18759
NM_017882.3(CLN6):c.*42T>G rs754655363 0.14249
NC_000015.10:g.68229772A>G rs541466473 0.12925
NM_017882.3(CLN6):c.298-196A>G rs61281446 0.07222
NM_017882.3(CLN6):c.298-248G>A rs59951468 0.07221
NM_017882.3(CLN6):c.486+51C>T rs8024979 0.07213
NM_017882.3(CLN6):c.83+35C>G rs150630197 0.05957
NM_017882.3(CLN6):c.198+181A>G rs59385667 0.03723
NM_017882.3(CLN6):c.486+8C>T rs149692285 0.01339
NM_017882.3(CLN6):c.34G>A (p.Ala12Thr) rs112239768 0.01081
NM_017882.3(CLN6):c.840G>A (p.Leu280=) rs148949069 0.00198
NM_017882.3(CLN6):c.214G>C (p.Glu72Gln) rs104894483 0.00140
NM_017882.3(CLN6):c.-38C>T rs756496671 0.00036
NM_017882.3(CLN6):c.42C>A (p.Gly14=) rs373776911 0.00036
NM_017882.3(CLN6):c.487-8T>C rs202046680 0.00019
NM_017882.3(CLN6):c.831C>T (p.Val277=) rs753344266 0.00003
NM_017882.2(CLN6):c.-178_-169delTCCGCTCCGC rs55672378
NM_017882.3(CLN6):c.*141GT[11] rs3837692
NM_017882.3(CLN6):c.*141GT[13] rs3837692
NM_017882.3(CLN6):c.*141GT[8] rs3837692
NM_017882.3(CLN6):c.195C>T (p.Ala65=) rs1472031434

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