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rs1057521080

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057521080(C;T)
Make rs1057521080(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position166037903
GeneSCN1A
is asnp
is mentioned by
dbSNPrs1057521080
dbSNP (old)rs1057521080
ClinGenrs1057521080
ebirs1057521080
HLIrs1057521080
Exacrs1057521080
Gnomadrs1057521080
Varsomers1057521080
Maprs1057521080
PheGenIrs1057521080
Biobankrs1057521080
1000 genomesrs1057521080
hgdprs1057521080
ensemblrs1057521080
gopubmedrs1057521080
geneviewrs1057521080
scholarrs1057521080
googlers1057521080
pharmgkbrs1057521080
gwascentralrs1057521080
openSNPrs1057521080
23andMers1057521080
23andMe allrs1057521080
SNPshotrs1057521080
SNPdbers1057521080
MSV3drs1057521080
GWAS Ctlgrs1057521080
Max Magnitude0
ClinVar
Risk rs1057521080(T;T)
Alt rs1057521080(T;T)
Reference Rs1057521080(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166894413G>A
CLNSRC
CLNACC RCV000428224.1,