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rs2082366

From SNPedia

Orientationminus
Stabilizedminus
Make rs2082366(C;C)
Make rs2082366(C;G)
Make rs2082366(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position165402907
is asnp
is mentioned by
dbSNPrs2082366
ebirs2082366
HLIrs2082366
Exacrs2082366
Varsomers2082366
Maprs2082366
PheGenIrs2082366
hapmaprs2082366
1000 genomesrs2082366
hgdprs2082366
ensemblrs2082366
gopubmedrs2082366
geneviewrs2082366
scholarrs2082366
googlers2082366
pharmgkbrs2082366
gwascentralrs2082366
openSNPrs2082366
23andMers2082366
23andMe allrs2082366
SNP Nexus

SNPshotrs2082366
SNPdbers2082366
MSV3drs2082366
GWAS Ctlgrs2082366
Max Magnitude
? (C;C) (C;G) (G;G) 28

[PMID 24337656] Case-control association study of polymorphisms in the voltage-gated sodium channel genes SCN1A, SCN2A, SCN3A, SCN1B, and SCN2B and epilepsy