ClinVar Miner

List of variants in gene DSP reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

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Gene type:
ClinVar version:
Total variants: 57
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HGVS dbSNP
NM_004415.3(DSP):c.-260A>G rs886061738
NM_004415.4(DSP):c.*112A>G rs141059005
NM_004415.4(DSP):c.*137T>C rs756543548
NM_004415.4(DSP):c.*289C>T rs886061749
NM_004415.4(DSP):c.*300C>A rs886061750
NM_004415.4(DSP):c.*305C>A rs886061751
NM_004415.4(DSP):c.*358A>T rs886061752
NM_004415.4(DSP):c.*384C>A rs886061753
NM_004415.4(DSP):c.*386G>T rs886061754
NM_004415.4(DSP):c.*577G>A rs886061755
NM_004415.4(DSP):c.*598G>T rs886061756
NM_004415.4(DSP):c.*681C>A rs886061757
NM_004415.4(DSP):c.-157G>A rs886061742
NM_004415.4(DSP):c.-179T>C rs886061741
NM_004415.4(DSP):c.-190G>T rs886061740
NM_004415.4(DSP):c.-228C>A rs886061739
NM_004415.4(DSP):c.-36C>A rs886061743
NM_004415.4(DSP):c.1469G>A (p.Arg490His) rs747815091
NM_004415.4(DSP):c.1743C>T (p.Ala581=) rs139095230
NM_004415.4(DSP):c.1840G>A (p.Asp614Asn) rs764951792
NM_004415.4(DSP):c.2377G>A (p.Glu793Lys) rs755067397
NM_004415.4(DSP):c.2404G>A (p.Asp802Asn) rs770105310
NM_004415.4(DSP):c.264C>T (p.Ile88=) rs727502997
NM_004415.4(DSP):c.2719C>T (p.Arg907Cys) rs749051278
NM_004415.4(DSP):c.2878-4G>A rs758303966
NM_004415.4(DSP):c.3146C>T (p.Ser1049Leu) rs751361395
NM_004415.4(DSP):c.3147G>A (p.Ser1049=) rs756341143
NM_004415.4(DSP):c.3303C>T (p.Tyr1101=) rs372440854
NM_004415.4(DSP):c.3389A>G (p.Asp1130Gly) rs886061746
NM_004415.4(DSP):c.3601G>A (p.Glu1201Lys) rs751566392
NM_004415.4(DSP):c.36C>T (p.Asn12=) rs886061744
NM_004415.4(DSP):c.4373G>A (p.Arg1458Gln) rs370063434
NM_004415.4(DSP):c.4478A>C (p.Glu1493Ala) rs760433367
NM_004415.4(DSP):c.4679A>G (p.Gln1560Arg) rs796530013
NM_004415.4(DSP):c.4857G>C (p.Leu1619=) rs373385083
NM_004415.4(DSP):c.5064G>A (p.Ala1688=) rs886061747
NM_004415.4(DSP):c.5217C>T (p.Ser1739=) rs748263306
NM_004415.4(DSP):c.5283C>T (p.Asn1761=) rs763355815
NM_004415.4(DSP):c.5316T>C (p.Asp1772=) rs376186141
NM_004415.4(DSP):c.5523A>C (p.Ser1841=) rs730882116
NM_004415.4(DSP):c.5544G>A (p.Arg1848=) rs727503004
NM_004415.4(DSP):c.5617C>T (p.Arg1873Cys) rs144392839
NM_004415.4(DSP):c.5820T>C (p.Asp1940=) rs763026647
NM_004415.4(DSP):c.5827A>G (p.Arg1943Gly) rs140663822
NM_004415.4(DSP):c.6307A>G (p.Lys2103Glu) rs149513743
NM_004415.4(DSP):c.6479G>A (p.Arg2160Gln) rs146642551
NM_004415.4(DSP):c.6935T>C (p.Val2312Ala) rs886061748
NM_004415.4(DSP):c.6968T>C (p.Ile2323Thr) rs777901747
NM_004415.4(DSP):c.7125G>A (p.Gly2375=) rs141709096
NM_004415.4(DSP):c.727-11T>C rs886061745
NM_004415.4(DSP):c.7622G>A (p.Arg2541Lys) rs142078450
NM_004415.4(DSP):c.8019C>T (p.Asp2673=) rs144275591
NM_004415.4(DSP):c.8217G>A (p.Pro2739=) rs755508926
NM_004415.4(DSP):c.8507G>A (p.Gly2836Glu) rs764232504
NM_004415.4(DSP):c.913A>G (p.Ile305Val) rs17604693
NM_004415.4(DSP):c.939C>T (p.Ser313=) rs766580649
NM_004415.4(DSP):c.9C>T (p.Cys3=) rs769032973

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