ClinVar Miner

List of variants in gene DIS3L2 reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (956):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 41
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HGVS dbSNP
NM_001257281.2(DIS3L2):c.1582-6629del rs373401005
NM_152383.4(DIS3L2):c.*103A>G rs113002914
NM_152383.4(DIS3L2):c.*13G>A rs200467865
NM_152383.4(DIS3L2):c.*255C>T rs143054885
NM_152383.4(DIS3L2):c.1011A>G (p.Leu337=) rs1553612378
NM_152383.4(DIS3L2):c.1056A>G (p.Leu352=) rs1286895716
NM_152383.4(DIS3L2):c.1170C>T (p.Leu390=) rs17272089
NM_152383.4(DIS3L2):c.1278G>A (p.Val426=) rs1488275564
NM_152383.4(DIS3L2):c.1448G>A (p.Arg483Gln) rs148474013
NM_152383.4(DIS3L2):c.1488T>C (p.His496=) rs72998118
NM_152383.4(DIS3L2):c.1638C>T (p.Asp546=) rs775532734
NM_152383.4(DIS3L2):c.1660-7T>C rs1553546465
NM_152383.4(DIS3L2):c.1707A>G (p.Gly569=) rs776261138
NM_152383.4(DIS3L2):c.1752G>A (p.Glu584=) rs1375650718
NM_152383.4(DIS3L2):c.1782C>G (p.Ala594=) rs765160562
NM_152383.4(DIS3L2):c.1800C>T (p.Ala600=) rs374119466
NM_152383.4(DIS3L2):c.1833C>A (p.Pro611=) rs747955751
NM_152383.4(DIS3L2):c.1836G>T (p.Pro612=) rs202227137
NM_152383.4(DIS3L2):c.1932G>C (p.Leu644=) rs1553550908
NM_152383.4(DIS3L2):c.1977G>A (p.Glu659=) rs1553550932
NM_152383.4(DIS3L2):c.2040G>T (p.Leu680=) rs751823544
NM_152383.4(DIS3L2):c.2073C>T (p.Leu691=) rs1413182287
NM_152383.4(DIS3L2):c.2187C>T (p.Pro729=) rs75782436
NM_152383.4(DIS3L2):c.2205G>A (p.Gln735=) rs549582540
NM_152383.4(DIS3L2):c.2253G>A (p.Glu751=) rs896293028
NM_152383.4(DIS3L2):c.237G>A (p.Lys79=) rs373861286
NM_152383.4(DIS3L2):c.2394+7G>A rs372069869
NM_152383.4(DIS3L2):c.2394+9C>T rs766054545
NM_152383.4(DIS3L2):c.2404C>T (p.Leu802=) rs1553552076
NM_152383.4(DIS3L2):c.2496+10C>T rs1553552123
NM_152383.4(DIS3L2):c.2628C>T (p.Asp876=) rs760111036
NM_152383.4(DIS3L2):c.264+9A>T rs745443608
NM_152383.4(DIS3L2):c.265-15C>A rs114804860
NM_152383.4(DIS3L2):c.34C>T (p.Pro12Ser) rs723044
NM_152383.4(DIS3L2):c.405T>C (p.Ala135=) rs1553606112
NM_152383.4(DIS3L2):c.426C>T (p.Pro142=) rs73001172
NM_152383.4(DIS3L2):c.456A>G (p.Gln152=) rs11887184
NM_152383.4(DIS3L2):c.558G>C (p.Leu186=) rs780991652
NM_152383.4(DIS3L2):c.703-9T>C rs1451942425
NM_152383.4(DIS3L2):c.723A>G (p.Lys241=) rs1553610349
NM_152383.4(DIS3L2):c.781C>T (p.Leu261=) rs1553610364

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