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rs1064795756

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome2
Position166002494
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs1064795756
dbSNP (old)rs1064795756
ClinGenrs1064795756
ebirs1064795756
HLIrs1064795756
Exacrs1064795756
Gnomadrs1064795756
Varsomers1064795756
Maprs1064795756
PheGenIrs1064795756
Biobankrs1064795756
1000 genomesrs1064795756
hgdprs1064795756
ensemblrs1064795756
gopubmedrs1064795756
geneviewrs1064795756
scholarrs1064795756
googlers1064795756
pharmgkbrs1064795756
gwascentralrs1064795756
openSNPrs1064795756
23andMers1064795756
23andMe allrs1064795756
SNPshotrs1064795756
SNPdbers1064795756
MSV3drs1064795756
GWAS Ctlgrs1064795756
Max Magnitude0
ClinVar
Risk rs1064795756(A;A)
Alt rs1064795756(A;A)
Reference Rs1064795756(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166859004C>T
CLNSRC
CLNACC RCV000481871.1,