ClinVar Miner

List of variants in gene DSP reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 119
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HGVS dbSNP
NM_004415.2(DSP):c.1045-8T>C rs201633815
NM_004415.2(DSP):c.1140+6T>C rs534740669
NM_004415.2(DSP):c.1920C>T (p.Ile640=) rs74806300
NM_004415.2(DSP):c.2121C>T (p.Asn707=) rs368590198
NM_004415.2(DSP):c.2360A>C (p.Tyr787Ser) rs778350289
NM_004415.2(DSP):c.2773C>T (p.Arg925Trp) rs145933612
NM_004415.2(DSP):c.3507C>T (p.Tyr1169=) rs148894066
NM_004415.2(DSP):c.3981C>T (p.Ile1327=) rs397516934
NM_004415.2(DSP):c.4041A>G (p.Glu1347=) rs200671552
NM_004415.2(DSP):c.4401A>G (p.Gln1467=) rs199818953
NM_004415.2(DSP):c.4741A>G (p.Lys1581Glu) rs186842903
NM_004415.2(DSP):c.4750G>A (p.Ala1584Thr) rs191778417
NM_004415.2(DSP):c.4752G>A (p.Ala1584=) rs201213622
NM_004415.2(DSP):c.4961T>C (p.Leu1654Pro) rs749730642
NM_004415.2(DSP):c.5178C>A (p.Asn1726Lys) rs147415451
NM_004415.2(DSP):c.522T>C (p.Cys174=) rs144781697
NM_004415.2(DSP):c.5304G>C (p.Gly1768=) rs530612211
NM_004415.2(DSP):c.5913G>T (p.Leu1971=) rs373416071
NM_004415.2(DSP):c.6655G>A (p.Val2219Ile) rs397516953
NM_004415.2(DSP):c.688G>A (p.Asp230Asn) rs147315869
NM_004415.2(DSP):c.6927G>A (p.Arg2309=) rs747248981
NM_004415.2(DSP):c.7077C>T (p.Ile2359=) rs966841386
NM_004415.2(DSP):c.7125G>A (p.Gly2375=) rs141709096
NM_004415.2(DSP):c.729C>T (p.Arg243=) rs141028505
NM_004415.2(DSP):c.7548G>A (p.Arg2516=) rs756527780
NM_004415.2(DSP):c.7557G>A (p.Leu2519=) rs397516957
NM_004415.2(DSP):c.7916G>A (p.Arg2639Gln) rs116888866
NM_004415.2(DSP):c.8019C>T (p.Asp2673=) rs144275591
NM_004415.2(DSP):c.8415C>T (p.Ala2805=) rs377148997
NM_004415.2(DSP):c.88G>A (p.Val30Met) rs121912998
NM_004415.3(DSP):c.-44G>A rs1041217575
NM_004415.3(DSP):c.1068G>A (p.Thr356=) rs766094745
NM_004415.3(DSP):c.1095C>G (p.Thr365=) rs1057520921
NM_004415.3(DSP):c.1154C>T (p.Ala385Val) rs146737031
NM_004415.3(DSP):c.1155G>A (p.Ala385=) rs140488069
NM_004415.3(DSP):c.12C>T (p.Asn4=) rs368802003
NM_004415.3(DSP):c.1308G>A (p.Gln436=) rs1057522715
NM_004415.3(DSP):c.1482C>T (p.Tyr494=) rs772925425
NM_004415.3(DSP):c.1542T>A (p.Pro514=) rs1554106920
NM_004415.3(DSP):c.1545G>A (p.Pro515=) rs747953037
NM_004415.3(DSP):c.1557C>T (p.Ala519=) rs769629611
NM_004415.3(DSP):c.1574+14G>T rs200443042
NM_004415.3(DSP):c.1575-15C>G rs369184165
NM_004415.3(DSP):c.1575-16C>G rs756806835
NM_004415.3(DSP):c.1575-4T>G rs745353405
NM_004415.3(DSP):c.1702-10C>A rs774406075
NM_004415.3(DSP):c.171-4T>C rs1554105598
NM_004415.3(DSP):c.1731G>A (p.Met577Ile) rs794728101
NM_004415.3(DSP):c.183G>A (p.Thr61=) rs150383703
NM_004415.3(DSP):c.1860G>A (p.Gln620=) rs762658467
NM_004415.3(DSP):c.1903+3delC rs1064793548
NM_004415.3(DSP):c.2023A>G (p.Ile675Val) rs142619902
NM_004415.3(DSP):c.2091A>T (p.Gly697=) rs2076304
NM_004415.3(DSP):c.2155A>C (p.Ile719Leu) rs1057520654
NM_004415.3(DSP):c.2297+14A>C rs1057520278
NM_004415.3(DSP):c.2298-10C>T rs1057522919
NM_004415.3(DSP):c.2298-16C>T rs1057521206
NM_004415.3(DSP):c.2316A>T (p.Ala772=) rs754896726
NM_004415.3(DSP):c.2436+16A>G rs199555263
NM_004415.3(DSP):c.2437-20T>G rs778134276
NM_004415.3(DSP):c.2596C>T (p.Arg866Cys) rs142429411
NM_004415.3(DSP):c.2631-5C>T rs773772683
NM_004415.3(DSP):c.2643G>A (p.Leu881=) rs1057520546
NM_004415.3(DSP):c.2793+18G>A rs1405091650
NM_004415.3(DSP):c.2793+19T>C rs778502149
NM_004415.3(DSP):c.2794-4dupA rs397516924
NM_004415.3(DSP):c.2794-7T>C rs397516926
NM_004415.3(DSP):c.2986-5C>T rs1554107902
NM_004415.3(DSP):c.2991A>C (p.Ala997=) rs780686578
NM_004415.3(DSP):c.3096C>T (p.Thr1032=) rs139199849
NM_004415.3(DSP):c.3147G>A (p.Ser1049=) rs756341143
NM_004415.3(DSP):c.3540A>G (p.Glu1180=) rs555514197
NM_004415.3(DSP):c.3642T>A (p.Ile1214=) rs755908729
NM_004415.3(DSP):c.3651G>A (p.Thr1217=) rs1057522191
NM_004415.3(DSP):c.3729A>G (p.Ser1243=) rs150241609
NM_004415.3(DSP):c.3843C>T (p.Gly1281=) rs757848395
NM_004415.3(DSP):c.3918T>C (p.Asn1306=) rs761749643
NM_004415.3(DSP):c.3954G>A (p.Lys1318=) rs866656949
NM_004415.3(DSP):c.3981C>A (p.Ile1327=) rs397516934
NM_004415.3(DSP):c.4500G>T (p.Leu1500=) rs372881903
NM_004415.3(DSP):c.4668C>T (p.Ile1556=) rs1299604004
NM_004415.3(DSP):c.4911G>A (p.Arg1637=) rs140620146
NM_004415.3(DSP):c.5005C>T (p.Leu1669Phe) rs794728102
NM_004415.3(DSP):c.5193C>T (p.Tyr1731=) rs201663619
NM_004415.3(DSP):c.5218G>A (p.Glu1740Lys) rs142885240
NM_004415.3(DSP):c.5257A>C (p.Arg1753=) rs775072446
NM_004415.3(DSP):c.5316T>C (p.Asp1772=) rs376186141
NM_004415.3(DSP):c.5463C>T (p.Val1821=) rs961915749
NM_004415.3(DSP):c.561C>T (p.Val187=) rs199585428
NM_004415.3(DSP):c.5958C>T (p.Ile1986=) rs577625038
NM_004415.3(DSP):c.598-4G>A rs747448946
NM_004415.3(DSP):c.6207C>T (p.Val2069=) rs147398792
NM_004415.3(DSP):c.6240C>T (p.Phe2080=) rs757650857
NM_004415.3(DSP):c.6319G>C (p.Val2107Leu) rs144263721
NM_004415.3(DSP):c.6351T>C (p.Asp2117=) rs148743859
NM_004415.3(DSP):c.6881C>G (p.Ala2294Gly) rs147000526
NM_004415.3(DSP):c.774G>C (p.Leu258=) rs753228677
NM_004415.3(DSP):c.782C>T (p.Ala261Val) rs139509870
NM_004415.3(DSP):c.7923C>T (p.Ile2641=) rs773906008
NM_004415.3(DSP):c.8024T>C (p.Val2675Ala) rs794728105
NM_004415.3(DSP):c.8097G>A (p.Glu2699=) rs1478062594
NM_004415.3(DSP):c.8199G>C (p.Thr2733=) rs145085696
NM_004415.3(DSP):c.8229G>A (p.Gly2743=) rs1060503979
NM_004415.3(DSP):c.8277C>T (p.Arg2759=) rs1248664648
NM_004415.3(DSP):c.837G>C (p.Thr279=) rs368051840
NM_004415.3(DSP):c.8394T>A (p.Thr2798=) rs775346694
NM_004415.3(DSP):c.8484_8495delCTCCCGCTCGGG (p.Ser2843_Arg2846del) rs1554109274
NM_004415.3(DSP):c.8487_8498delCCGCTCGGGATC (p.Ser2843_Arg2846del) rs727504704
NM_004415.3(DSP):c.8493G>C (p.Ser2831=) rs397516969
NM_004415.3(DSP):c.8508A>G (p.Gly2836=) rs754074127
NM_004415.3(DSP):c.8508_8519delATCTCGCTCCGG (p.Ser2843_Arg2846del) rs397516971
NM_004415.3(DSP):c.8511T>C (p.Ser2837=) rs757475874
NM_004415.3(DSP):c.8515_8517delTCCinsAGT (p.Ser2839=) rs1554109285
NM_004415.3(DSP):c.8580T>C (p.Tyr2860=) rs201441128
NM_004415.3(DSP):c.867C>T (p.Cys289=) rs397516973
NM_004415.3(DSP):c.915C>T (p.Ile305=) rs148395326
NM_004415.3(DSP):c.939+16G>A rs781034092
NM_004415.3(DSP):c.939+17C>T rs140481492
NM_004415.3(DSP):c.987G>A (p.Leu329=) rs564435126

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