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rs1057518325

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057518325(C;C)
Make rs1057518325(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position166037795
GeneSCN1A
is asnp
is mentioned by
dbSNPrs1057518325
dbSNP (old)rs1057518325
ClinGenrs1057518325
ebirs1057518325
HLIrs1057518325
Exacrs1057518325
Gnomadrs1057518325
Varsomers1057518325
Maprs1057518325
PheGenIrs1057518325
Biobankrs1057518325
1000 genomesrs1057518325
hgdprs1057518325
ensemblrs1057518325
gopubmedrs1057518325
geneviewrs1057518325
scholarrs1057518325
googlers1057518325
pharmgkbrs1057518325
gwascentralrs1057518325
openSNPrs1057518325
23andMers1057518325
23andMe allrs1057518325
SNPshotrs1057518325
SNPdbers1057518325
MSV3drs1057518325
GWAS Ctlgrs1057518325
Max Magnitude0
ClinVar
Risk rs1057518325(C;C)
Alt rs1057518325(C;C)
Reference Rs1057518325(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166894305A>G
CLNSRC
CLNACC RCV000413254.1,