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rs1057517849

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517849(G;T)
Make rs1057517849(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position166039422
GeneSCN1A
is asnp
is mentioned by
dbSNPrs1057517849
dbSNP (old)rs1057517849
ClinGenrs1057517849
ebirs1057517849
HLIrs1057517849
Exacrs1057517849
Gnomadrs1057517849
Varsomers1057517849
Maprs1057517849
PheGenIrs1057517849
Biobankrs1057517849
1000 genomesrs1057517849
hgdprs1057517849
ensemblrs1057517849
gopubmedrs1057517849
geneviewrs1057517849
scholarrs1057517849
googlers1057517849
pharmgkbrs1057517849
gwascentralrs1057517849
openSNPrs1057517849
23andMers1057517849
23andMe allrs1057517849
SNPshotrs1057517849
SNPdbers1057517849
MSV3drs1057517849
GWAS Ctlgrs1057517849
Max Magnitude0
ClinVar
Risk rs1057517849(T;T)
Alt rs1057517849(T;T)
Reference Rs1057517849(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166895932C>A
CLNSRC
CLNACC RCV000413444.1,