ClinVar Miner

List of variants in gene combination SCN1A, SCN9A reported as likely benign by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 47
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001365536.1(SCN9A):c.2190G>C (p.Trp730Cys) rs202055175 0.00320
NM_001365536.1(SCN9A):c.5779C>T (p.Leu1927Phe) rs111558968 0.00315
NM_001365536.1(SCN9A):c.2248A>G (p.Ile750Val) rs182650126 0.00270
NM_001365536.1(SCN9A):c.4356C>T (p.Phe1452=) rs201145311 0.00245
NM_001365536.1(SCN9A):c.3506A>C (p.Asn1169Thr) rs151241025 0.00216
NM_001365536.1(SCN9A):c.4645T>C (p.Trp1549Arg) rs202084411 0.00190
NM_001365536.1(SCN9A):c.1997A>G (p.Lys666Arg) rs121908919 0.00176
NM_001365536.1(SCN9A):c.3832C>G (p.Leu1278Val) rs180922748 0.00174
NM_001365536.1(SCN9A):c.3509T>C (p.Ile1170Thr) rs73019664 0.00128
NM_001365536.1(SCN9A):c.2409T>C (p.Tyr803=) rs142219317 0.00101
NM_001365536.1(SCN9A):c.3195C>T (p.Ser1065=) rs111674454 0.00096
NM_001365536.1(SCN9A):c.1326G>A (p.Ala442=) rs200065104 0.00092
NM_001365536.1(SCN9A):c.2766C>T (p.Arg922=) rs199653503 0.00088
NM_001365536.1(SCN9A):c.3020G>A (p.Arg1007His) rs188145203 0.00075
NM_001365536.1(SCN9A):c.1464C>T (p.Leu488=) rs200682458 0.00058
NM_001365536.1(SCN9A):c.3801T>C (p.Asp1267=) rs202047865 0.00042
NM_001365536.1(SCN9A):c.3684T>C (p.Tyr1228=) rs144941725 0.00036
NM_001365536.1(SCN9A):c.2964C>T (p.Leu988=) rs201430964 0.00035
NM_001365536.1(SCN9A):c.1980G>A (p.Thr660=) rs200014315 0.00023
NM_001365536.1(SCN9A):c.4110T>C (p.Cys1370=) rs199673396 0.00020
NM_001365536.1(SCN9A):c.1177C>T (p.Leu393=) rs184773311 0.00018
NM_001365536.1(SCN9A):c.1110G>A (p.Thr370=) rs202002028 0.00016
NM_001365536.1(SCN9A):c.3573C>T (p.His1191=) rs375710841 0.00016
NM_001365536.1(SCN9A):c.5711G>A (p.Arg1904His) rs79805025 0.00016
NM_001365536.1(SCN9A):c.3228T>A (p.Gly1076=) rs200393050 0.00013
NM_001365536.1(SCN9A):c.3207C>T (p.His1069=) rs200689065 0.00010
NM_001365536.1(SCN9A):c.965+13T>C rs772337722 0.00010
NM_001365536.1(SCN9A):c.2165T>C (p.Leu722Ser) rs187526567 0.00009
NM_001365536.1(SCN9A):c.2634C>T (p.Phe878=) rs188678956 0.00008
NM_001365536.1(SCN9A):c.3802-13del rs747729984 0.00007
NM_001365536.1(SCN9A):c.2461G>A (p.Val821Met) rs41268671 0.00006
NM_001365536.1(SCN9A):c.1975-8T>A rs752961542 0.00005
NM_001365536.1(SCN9A):c.3540C>T (p.Asn1180=) rs766241126 0.00003
NM_001365536.1(SCN9A):c.966-8G>A rs199942413 0.00003
NM_001365536.1(SCN9A):c.1602+15G>T rs201987507 0.00002
NM_001365536.1(SCN9A):c.4261-13G>C rs745685331 0.00002
NM_001365536.1(SCN9A):c.5586G>A (p.Gln1862=) rs199572382 0.00002
NM_001365536.1(SCN9A):c.1107+7A>G rs199623041 0.00001
NM_001365536.1(SCN9A):c.2253C>T (p.Thr751=) rs751536693 0.00001
NM_001365536.1(SCN9A):c.2712G>A (p.Thr904=) rs200494981 0.00001
NM_001365536.1(SCN9A):c.3036A>G (p.Lys1012=) rs200375962 0.00001
NM_001365536.1(SCN9A):c.3807T>A (p.Ser1269=) rs1272510761 0.00001
NM_001365536.1(SCN9A):c.2875-18C>T rs1553486847
NM_001365536.1(SCN9A):c.3351+15T>C rs763278343
NM_001365536.1(SCN9A):c.3834T>G (p.Leu1278=) rs1553480111
NM_001365536.1(SCN9A):c.4141C>A (p.Arg1381=) rs748159444
NM_001365536.1(SCN9A):c.965+18T>C rs1553492740

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.