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rs1057519525

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519525(G;G)
Make rs1057519525(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position165308760
GeneSCN2A
is asnp
is mentioned by
dbSNPrs1057519525
dbSNP (old)rs1057519525
ClinGenrs1057519525
ebirs1057519525
HLIrs1057519525
Exacrs1057519525
Gnomadrs1057519525
Varsomers1057519525
Maprs1057519525
PheGenIrs1057519525
Biobankrs1057519525
1000 genomesrs1057519525
hgdprs1057519525
ensemblrs1057519525
gopubmedrs1057519525
geneviewrs1057519525
scholarrs1057519525
googlers1057519525
pharmgkbrs1057519525
gwascentralrs1057519525
openSNPrs1057519525
23andMers1057519525
23andMe allrs1057519525
SNPshotrs1057519525
SNPdbers1057519525
MSV3drs1057519525
GWAS Ctlgrs1057519525
Max Magnitude0
ClinVar
Risk rs1057519525(G;G)
Alt rs1057519525(G;G)
Reference Rs1057519525(T;T)
Significance Probable-Pathogenic
Disease Focal epilepsy
Variation info
Gene SCN2A
CLNDBN Focal epilepsy
Reversed 0
HGVS NC_000002.11:g.166165270T>G
CLNSRC
CLNACC RCV000416990.1,