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rs1057518094

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057518094(A;C)
Make rs1057518094(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position166047707
GeneSCN1A
is asnp
is mentioned by
dbSNPrs1057518094
dbSNP (old)rs1057518094
ClinGenrs1057518094
ebirs1057518094
HLIrs1057518094
Exacrs1057518094
Gnomadrs1057518094
Varsomers1057518094
Maprs1057518094
PheGenIrs1057518094
Biobankrs1057518094
1000 genomesrs1057518094
hgdprs1057518094
ensemblrs1057518094
gopubmedrs1057518094
geneviewrs1057518094
scholarrs1057518094
googlers1057518094
pharmgkbrs1057518094
gwascentralrs1057518094
openSNPrs1057518094
23andMers1057518094
23andMe allrs1057518094
SNPshotrs1057518094
SNPdbers1057518094
MSV3drs1057518094
GWAS Ctlgrs1057518094
Max Magnitude0
ClinVar
Risk rs1057518094(C;C)
Alt rs1057518094(C;C)
Reference Rs1057518094(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166904217T>G
CLNSRC
CLNACC RCV000414158.1,