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rs1057518110

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057518110(C;C)
Make rs1057518110(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position166038116
GeneSCN1A
is asnp
is mentioned by
dbSNPrs1057518110
dbSNP (old)rs1057518110
ClinGenrs1057518110
ebirs1057518110
HLIrs1057518110
Exacrs1057518110
Gnomadrs1057518110
Varsomers1057518110
Maprs1057518110
PheGenIrs1057518110
Biobankrs1057518110
1000 genomesrs1057518110
hgdprs1057518110
ensemblrs1057518110
gopubmedrs1057518110
geneviewrs1057518110
scholarrs1057518110
googlers1057518110
pharmgkbrs1057518110
gwascentralrs1057518110
openSNPrs1057518110
23andMers1057518110
23andMe allrs1057518110
SNPshotrs1057518110
SNPdbers1057518110
MSV3drs1057518110
GWAS Ctlgrs1057518110
Max Magnitude0
ClinVar
Risk rs1057518110(C;C)
Alt rs1057518110(C;C)
Reference Rs1057518110(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166894626A>G
CLNSRC
CLNACC RCV000413718.1,