ClinVar Miner

List of variants in gene DSP reported as uncertain significance for Cardiovascular phenotype

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Total variants: 74
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HGVS dbSNP
NM_004415.4(DSP):c.106G>A (p.Gly36Ser) rs1395509692
NM_004415.4(DSP):c.1090A>G (p.Ile364Val) rs886038909
NM_004415.4(DSP):c.1102A>T (p.Ile368Phe) rs794728112
NM_004415.4(DSP):c.1180G>A (p.Gly394Arg) rs769054351
NM_004415.4(DSP):c.1274G>A (p.Arg425Gln) rs397516916
NM_004415.4(DSP):c.1331A>C (p.Lys444Thr) rs1554106843
NM_004415.4(DSP):c.1469G>A (p.Arg490His) rs747815091
NM_004415.4(DSP):c.146C>G (p.Thr49Ser) rs151153655
NM_004415.4(DSP):c.1483G>A (p.Val495Met) rs372014020
NM_004415.4(DSP):c.1696G>A (p.Ala566Thr) rs148147581
NM_004415.4(DSP):c.171-4T>C rs1554105598
NM_004415.4(DSP):c.1778A>G (p.Asn593Ser) rs34239595
NM_004415.4(DSP):c.1865T>G (p.Leu622Arg) rs1554107098
NM_004415.4(DSP):c.2047G>A (p.Glu683Lys) rs775181391
NM_004415.4(DSP):c.2122G>A (p.Glu708Lys) rs773113261
NM_004415.4(DSP):c.2159C>G (p.Ala720Gly) rs1261146655
NM_004415.4(DSP):c.2168T>C (p.Leu723Pro) rs1554107443
NM_004415.4(DSP):c.2234A>C (p.Glu745Ala) rs969462343
NM_004415.4(DSP):c.2546A>G (p.Tyr849Cys) rs778636665
NM_004415.4(DSP):c.2622C>G (p.Ile874Met) rs751067479
NM_004415.4(DSP):c.2723G>A (p.Arg908His) rs142494121
NM_004415.4(DSP):c.2747A>C (p.Lys916Thr) rs1554107730
NM_004415.4(DSP):c.2774G>A (p.Arg925Gln) rs139799237
NM_004415.4(DSP):c.2799G>C (p.Leu933Phe) rs372922674
NM_004415.4(DSP):c.2866A>T (p.Asn956Tyr) rs397516928
NM_004415.4(DSP):c.3025A>G (p.Arg1009Gly) rs1413346143
NM_004415.4(DSP):c.3294C>G (p.Asp1098Glu) rs535762713
NM_004415.4(DSP):c.344A>G (p.Asn115Ser) rs28763958
NM_004415.4(DSP):c.3661A>G (p.Ile1221Val) rs794728120
NM_004415.4(DSP):c.3862A>C (p.Lys1288Gln) rs138907450
NM_004415.4(DSP):c.3877A>G (p.Ile1293Val) rs376555665
NM_004415.4(DSP):c.3905G>A (p.Arg1302His) rs760691999
NM_004415.4(DSP):c.3922C>T (p.Arg1308Trp) rs144641271
NM_004415.4(DSP):c.3971A>T (p.Asn1324Ile) rs749820299
NM_004415.4(DSP):c.3973A>C (p.Lys1325Gln) rs41302883
NM_004415.4(DSP):c.4332A>C (p.Lys1444Asn) rs1374798133
NM_004415.4(DSP):c.4352T>C (p.Leu1451Pro) rs1554108296
NM_004415.4(DSP):c.4527_4559del (p.Arg1509_Ser1519del) rs397516939
NM_004415.4(DSP):c.4741A>G (p.Lys1581Glu) rs186842903
NM_004415.4(DSP):c.4886G>T (p.Ser1629Ile) rs200243976
NM_004415.4(DSP):c.5161_5163GAA[2] (p.Glu1723del) rs730880091
NM_004415.4(DSP):c.5167G>C (p.Glu1723Gln) rs142803672
NM_004415.4(DSP):c.5285G>A (p.Arg1762Gln) rs751849031
NM_004415.4(DSP):c.5351T>C (p.Ile1784Thr) rs1554108491
NM_004415.4(DSP):c.5383T>A (p.Ser1795Thr) rs764279057
NM_004415.4(DSP):c.5542A>G (p.Arg1848Gly) rs886038805
NM_004415.4(DSP):c.5554C>T (p.Arg1852Cys) rs550818559
NM_004415.4(DSP):c.5555G>A (p.Arg1852His) rs193922669
NM_004415.4(DSP):c.598-4G>A rs747448946
NM_004415.4(DSP):c.6010G>T (p.Val2004Phe) rs764692193
NM_004415.4(DSP):c.6062C>G (p.Ala2021Gly) rs760673242
NM_004415.4(DSP):c.6187C>G (p.Arg2063Gly) rs374090050
NM_004415.4(DSP):c.6188G>A (p.Arg2063Gln) rs142927608
NM_004415.4(DSP):c.61G>A (p.Glu21Lys) rs747956457
NM_004415.4(DSP):c.6284G>A (p.Gly2095Asp) rs1554108784
NM_004415.4(DSP):c.6295_6296delinsAT (p.Pro2099Ile) rs587782942
NM_004415.4(DSP):c.6772A>G (p.Ser2258Gly) rs886038842
NM_004415.4(DSP):c.6902T>C (p.Ile2301Thr) rs772381363
NM_004415.4(DSP):c.7347_7349GAA[1] (p.Lys2451del) rs766860183
NM_004415.4(DSP):c.7451A>G (p.Lys2484Arg) rs1346398330
NM_004415.4(DSP):c.7534G>T (p.Asp2512Tyr) rs772574987
NM_004415.4(DSP):c.7575C>T (p.Gly2525=) rs780156504
NM_004415.4(DSP):c.7738G>T (p.Asp2580Tyr) rs371129517
NM_004415.4(DSP):c.782C>T (p.Ala261Val) rs139509870
NM_004415.4(DSP):c.7994C>T (p.Thr2665Met) rs151309106
NM_004415.4(DSP):c.8111_8113AGA[2] (p.Lys2706del) rs397516962
NM_004415.4(DSP):c.8209G>C (p.Val2737Leu) rs149123428
NM_004415.4(DSP):c.8281G>A (p.Ala2761Thr) rs376751288
NM_004415.4(DSP):c.8462C>T (p.Ser2821Leu) rs201826850
NM_004415.4(DSP):c.8467C>G (p.Pro2823Ala) rs142717240
NM_004415.4(DSP):c.8493_8504dup (p.2827_2830SGSR[6]) rs748194022
NM_004415.4(DSP):c.8591T>A (p.Phe2864Tyr) rs1554109334
NM_004415.4(DSP):c.913A>G (p.Ile305Val) rs17604693
NM_004415.4(DSP):c.943C>T (p.Arg315Cys) rs200476515

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