ClinVar Miner

List of variants in gene DSP reported as benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 84
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HGVS dbSNP
NC_000006.12:g.7541350G>A
NC_000006.12:g.7541378G>C
NC_000006.12:g.7578160_7578163del
NM_004415.4(DSP):c.1141-44C>T rs2076296
NM_004415.4(DSP):c.1206G>A (p.Lys402=) rs150422458
NM_004415.4(DSP):c.1266+215G>T
NM_004415.4(DSP):c.1266+6G>T rs73375345
NM_004415.4(DSP):c.12C>G (p.Asn4Lys) rs368802003
NM_004415.4(DSP):c.1344G>A (p.Leu448=) rs138226280
NM_004415.4(DSP):c.1420-93C>T
NM_004415.4(DSP):c.1481A>T (p.Tyr494Phe) rs28763961
NM_004415.4(DSP):c.170+163C>T
NM_004415.4(DSP):c.170+300C>A
NM_004415.4(DSP):c.1701+167A>G
NM_004415.4(DSP):c.1701+186C>G
NM_004415.4(DSP):c.1702-289G>T
NM_004415.4(DSP):c.171-285A>G
NM_004415.4(DSP):c.171-315_171-314insTATT
NM_004415.4(DSP):c.1903+57G>A
NM_004415.4(DSP):c.1903+7T>C rs28763962
NM_004415.4(DSP):c.1904-49T>A rs2076303
NM_004415.4(DSP):c.1dup (p.Met1fs) rs17133512
NM_004415.4(DSP):c.2297+51T>C
NM_004415.4(DSP):c.2298-38T>C
NM_004415.4(DSP):c.2298-85C>T
NM_004415.4(DSP):c.237C>T (p.Ser79=) rs146521568
NM_004415.4(DSP):c.2630+18C>T rs145963404
NM_004415.4(DSP):c.2631-159G>A
NM_004415.4(DSP):c.2673T>C (p.Tyr891=) rs146407262
NM_004415.4(DSP):c.2723G>A (p.Arg908His) rs142494121
NM_004415.4(DSP):c.273+180G>T
NM_004415.4(DSP):c.273+191A>G
NM_004415.4(DSP):c.274-285dup
NM_004415.4(DSP):c.274-309A>G
NM_004415.4(DSP):c.274-31T>C rs10484326
NM_004415.4(DSP):c.2794-113G>A
NM_004415.4(DSP):c.2815G>A (p.Gly939Ser) rs80325569
NM_004415.4(DSP):c.2877+79C>A
NM_004415.4(DSP):c.2878-268A>G
NM_004415.4(DSP):c.2985+224G>C
NM_004415.4(DSP):c.2985+70G>A
NM_004415.4(DSP):c.2986-6T>A rs144748036
NM_004415.4(DSP):c.3018A>G (p.Leu1006=) rs375412541
NM_004415.4(DSP):c.3084+175C>T
NM_004415.4(DSP):c.3084+24T>G rs2806229
NM_004415.4(DSP):c.3084+28G>A rs2842691
NM_004415.4(DSP):c.3085-114A>G
NM_004415.4(DSP):c.3085-115C>T
NM_004415.4(DSP):c.3085-145A>T
NM_004415.4(DSP):c.3085-197G>T
NM_004415.4(DSP):c.3510G>A (p.Glu1170=) rs28763964
NM_004415.4(DSP):c.3696C>A (p.Ser1232=) rs141120358
NM_004415.4(DSP):c.4141A>T (p.Thr1381Ser) rs77758574
NM_004415.4(DSP):c.422+275G>A
NM_004415.4(DSP):c.423-16_423-15insC rs113028223
NM_004415.4(DSP):c.4383G>A (p.Glu1461=) rs140029036
NM_004415.4(DSP):c.4455G>T (p.Arg1485Ser) rs113902911
NM_004415.4(DSP):c.4489C>T (p.Arg1497Trp) rs148041814
NM_004415.4(DSP):c.4588G>T (p.Val1530Phe) rs141227126
NM_004415.4(DSP):c.5498A>T (p.Glu1833Val) rs78652302
NM_004415.4(DSP):c.6192T>C (p.Asn2064=) rs371230455
NM_004415.4(DSP):c.6208G>A (p.Asp2070Asn) rs41302885
NM_004415.4(DSP):c.6381C>T (p.Ala2127=) rs146315412
NM_004415.4(DSP):c.6753G>A (p.Lys2251=) rs750294829
NM_004415.4(DSP):c.726+219T>G
NM_004415.4(DSP):c.727-206C>T
NM_004415.4(DSP):c.727-213G>A
NM_004415.4(DSP):c.741G>A (p.Ala247=) rs2806234
NM_004415.4(DSP):c.7734C>T (p.Ser2578=) rs28763970
NM_004415.4(DSP):c.777+104G>A
NM_004415.4(DSP):c.777+120C>G
NM_004415.4(DSP):c.7995G>A (p.Thr2665=) rs35379048
NM_004415.4(DSP):c.8191T>C (p.Tyr2731His) rs201397978
NM_004415.4(DSP):c.8268A>C (p.Ile2756=) rs397516963
NM_004415.4(DSP):c.8300C>A (p.Thr2767Asn) rs34884895
NM_004415.4(DSP):c.8301C>G (p.Thr2767=) rs145362059
NM_004415.4(DSP):c.8455A>C (p.Met2819Leu) rs138329459
NM_004415.4(DSP):c.8481C>T (p.Ser2827=) rs151029175
NM_004415.4(DSP):c.8605A>G (p.Ile2869Val) rs28763971
NM_004415.4(DSP):c.939+132G>A
NM_004415.4(DSP):c.939+195G>A
NM_004415.4(DSP):c.939+299C>T
NM_004415.4(DSP):c.940-195T>C
NM_004415.4(DSP):c.940-224T>C

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