ClinVar Miner

List of variants in gene combination SCN1A, SCN9A reported as benign for Indifference to pain, congenital, autosomal recessive

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Gene type:
ClinVar version:
Total variants: 44
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HGVS dbSNP
NM_001365536.1(SCN9A):c.*1013C>T rs16851754
NM_001365536.1(SCN9A):c.*1184T>G rs11902920
NM_001365536.1(SCN9A):c.*125C>T rs200465050
NM_001365536.1(SCN9A):c.*129C>T rs16851759
NM_001365536.1(SCN9A):c.*1492C>G rs73017542
NM_001365536.1(SCN9A):c.*1660G>A rs16851753
NM_001365536.1(SCN9A):c.*1774G>A rs114843828
NM_001365536.1(SCN9A):c.*1796C>T rs16851751
NM_001365536.1(SCN9A):c.*18A>G rs150401869
NM_001365536.1(SCN9A):c.*204G>A rs111510277
NM_001365536.1(SCN9A):c.*2136C>G rs77050817
NM_001365536.1(SCN9A):c.*2146G>C rs1062844
NM_001365536.1(SCN9A):c.*2154C>G rs17804037
NM_001365536.1(SCN9A):c.*2155G>A rs77565541
NM_001365536.1(SCN9A):c.*2297A>T rs75345520
NM_001365536.1(SCN9A):c.*2323G>T rs142172527
NM_001365536.1(SCN9A):c.*235T>C rs140553451
NM_001365536.1(SCN9A):c.*237C>G rs16851755
NM_001365536.1(SCN9A):c.*2540C>T rs58249489
NM_001365536.1(SCN9A):c.*2640G>A rs13396526
NM_001365536.1(SCN9A):c.*2662G>A rs149873320
NM_001365536.1(SCN9A):c.*2854T>C rs73017538
NM_001365536.1(SCN9A):c.*377C>G rs115464654
NM_001365536.1(SCN9A):c.*958C>T rs143727895
NM_001365536.1(SCN9A):c.1119T>C (p.Ala373=) rs13414203
NM_001365536.1(SCN9A):c.1155G>T (p.Val385=) rs58465962
NM_001365536.1(SCN9A):c.1266A>G (p.Glu422=) rs13402180
NM_001365536.1(SCN9A):c.1287T>A (p.Arg429=) rs6747673
NM_001365536.1(SCN9A):c.1469G>A (p.Ser490Asn) rs58022607
NM_001365536.1(SCN9A):c.1828C>A (p.Pro610Thr) rs41268673
NM_001365536.1(SCN9A):c.2105-14C>T rs6432893
NM_001365536.1(SCN9A):c.2105-15G>A rs4525717
NM_001365536.1(SCN9A):c.2165T>C (p.Leu722Ser) rs187526567
NM_001365536.1(SCN9A):c.2392A>G (p.Met798Val) rs149707354
NM_001365536.1(SCN9A):c.2437A>G (p.Ser813Gly) rs201890240
NM_001365536.1(SCN9A):c.2827A>C (p.Met943Leu) rs12478318
NM_001365536.1(SCN9A):c.3004G>T (p.Val1002Leu) rs4369876
NM_001365536.1(SCN9A):c.3362G>A (p.Arg1121Gln) rs74401238
NM_001365536.1(SCN9A):c.3675C>A (p.Ile1225=) rs77144869
NM_001365536.1(SCN9A):c.3802-4A>G rs75230218
NM_001365536.1(SCN9A):c.3802-8T>C rs76550960
NM_001365536.1(SCN9A):c.4399-14G>T rs112927502
NM_001365536.1(SCN9A):c.4812G>T (p.Val1604=) rs149207258
NM_001365536.1(SCN9A):c.5756A>G (p.Asp1919Gly) rs3750904

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