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rs10188577

From SNPedia

Orientationplus
Stabilizedplus
Make rs10188577(C;C)
Make rs10188577(C;T)
Make rs10188577(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position166059387
GeneSCN1A
is asnp
is mentioned by
dbSNPrs10188577
ebirs10188577
HLIrs10188577
Exacrs10188577
Varsomers10188577
Maprs10188577
PheGenIrs10188577
hapmaprs10188577
1000 genomesrs10188577
hgdprs10188577
ensemblrs10188577
gopubmedrs10188577
geneviewrs10188577
scholarrs10188577
googlers10188577
pharmgkbrs10188577
gwascentralrs10188577
openSNPrs10188577
23andMers10188577
23andMe allrs10188577
SNP Nexus

SNPshotrs10188577
SNPdbers10188577
MSV3drs10188577
GWAS Ctlgrs10188577
Max Magnitude
? (C;C) (C;T) (T;T) 28

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


[PMID 24342961] SCN1A variations and response to multiple antiepileptic drugs