ClinVar Miner

List of variants in gene combination LOC102724058, SCN1A reported as benign for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 28
Download table as spreadsheet
HGVS dbSNP
NM_006920.6(SCN1A):c.*20A>G rs565537621
NM_006920.6(SCN1A):c.3166G>A (p.Ala1056Thr) rs2298771
NM_006920.6(SCN1A):c.3297T>C (p.Ser1099=) rs587781145
NM_006920.6(SCN1A):c.3465G>A (p.Gln1155=) rs145410000
NM_006920.6(SCN1A):c.3517+11G>T rs202142409
NM_006920.6(SCN1A):c.3672+10del rs570862962
NM_006920.6(SCN1A):c.3672+12T>G rs147032678
NM_006920.6(SCN1A):c.3690T>C (p.Tyr1230=) rs36031496
NM_006920.6(SCN1A):c.3771T>C (p.Leu1257=) rs143980709
NM_006920.6(SCN1A):c.3853T>C (p.Leu1285=) rs375896308
NM_006920.6(SCN1A):c.3915G>A (p.Arg1305=) rs149579028
NM_006920.6(SCN1A):c.4284T>C (p.Tyr1428=) rs758014915
NM_006920.6(SCN1A):c.4353C>T (p.Tyr1451=) rs587781146
NM_006920.6(SCN1A):c.4360A>G (p.Ile1454Val) rs138231868
NM_006920.6(SCN1A):c.4473A>G (p.Glu1491=) rs587781147
NM_006920.6(SCN1A):c.4515G>A (p.Ser1505=) rs78041051
NM_006920.6(SCN1A):c.4524G>A (p.Pro1508=) rs368785509
NM_006920.6(SCN1A):c.4691G>A (p.Arg1564His) rs368834365
NM_006920.6(SCN1A):c.4698T>C (p.Asn1566=) rs145296488
NM_006920.6(SCN1A):c.4822A>G (p.Met1608Val) rs373967247
NM_006920.6(SCN1A):c.4839G>A (p.Leu1613=) rs142910512
NM_006920.6(SCN1A):c.4912C>T (p.Leu1638=) rs148546224
NM_006920.6(SCN1A):c.5253A>G (p.Gly1751=) rs150570058
NM_006920.6(SCN1A):c.5313C>T (p.Ile1771=) rs121918763
NM_006920.6(SCN1A):c.5323C>T (p.Leu1775=) rs587781148
NM_006920.6(SCN1A):c.5385G>A (p.Glu1795=) rs140237315
NM_006920.6(SCN1A):c.5733T>C (p.Ile1911=) rs587781149
NM_006920.6(SCN1A):c.5831T>C (p.Ile1944Thr) rs35735053

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.