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rs1057517862

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517862(A;A)
Make rs1057517862(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position166038128
GeneSCN1A
is asnp
is mentioned by
dbSNPrs1057517862
dbSNP (old)rs1057517862
ClinGenrs1057517862
ebirs1057517862
HLIrs1057517862
Exacrs1057517862
Gnomadrs1057517862
Varsomers1057517862
Maprs1057517862
PheGenIrs1057517862
Biobankrs1057517862
1000 genomesrs1057517862
hgdprs1057517862
ensemblrs1057517862
gopubmedrs1057517862
geneviewrs1057517862
scholarrs1057517862
googlers1057517862
pharmgkbrs1057517862
gwascentralrs1057517862
openSNPrs1057517862
23andMers1057517862
23andMe allrs1057517862
SNPshotrs1057517862
SNPdbers1057517862
MSV3drs1057517862
GWAS Ctlgrs1057517862
Max Magnitude0
ClinVar
Risk rs1057517862(A;A)
Alt rs1057517862(A;A)
Reference Rs1057517862(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166894638C>T
CLNSRC
CLNACC RCV000413258.1,