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rs1064796123

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AG;AG) 0 common in clinvar
Chromosome2
Position165314089
GeneSCN2A
is asnp
is mentioned by
dbSNPrs1064796123
dbSNP (old)rs1064796123
ClinGenrs1064796123
ebirs1064796123
HLIrs1064796123
Exacrs1064796123
Gnomadrs1064796123
Varsomers1064796123
LitVarrs1064796123
Maprs1064796123
PheGenIrs1064796123
Biobankrs1064796123
1000 genomesrs1064796123
hgdprs1064796123
ensemblrs1064796123
gopubmedrs1064796123
geneviewrs1064796123
scholarrs1064796123
googlers1064796123
pharmgkbrs1064796123
gwascentralrs1064796123
openSNPrs1064796123
23andMers1064796123
23andMe allrs1064796123
SNPshotrs1064796123
SNPdbers1064796123
MSV3drs1064796123
GWAS Ctlgrs1064796123
Max Magnitude0
ClinVar
Risk rs1064796123(T;T)
Alt rs1064796123(T;T)
Reference Rs1064796123(AG;AG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166170599_166170600delAGinsT
CLNSRC
CLNACC RCV000487214.1,