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rs1057517959

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517959(A;A)
Make rs1057517959(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position166041284
GeneSCN1A
is asnp
is mentioned by
dbSNPrs1057517959
dbSNP (old)rs1057517959
ClinGenrs1057517959
ebirs1057517959
HLIrs1057517959
Exacrs1057517959
Gnomadrs1057517959
Varsomers1057517959
Maprs1057517959
PheGenIrs1057517959
Biobankrs1057517959
1000 genomesrs1057517959
hgdprs1057517959
ensemblrs1057517959
gopubmedrs1057517959
geneviewrs1057517959
scholarrs1057517959
googlers1057517959
pharmgkbrs1057517959
gwascentralrs1057517959
openSNPrs1057517959
23andMers1057517959
23andMe allrs1057517959
SNPshotrs1057517959
SNPdbers1057517959
MSV3drs1057517959
GWAS Ctlgrs1057517959
Max Magnitude0
ClinVar
Risk rs1057517959(A;A)
Alt rs1057517959(A;A)
Reference Rs1057517959(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166897794C>T
CLNSRC
CLNACC RCV000413156.1,