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rs1064796203

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome2
Position165354663
GeneSCN2A
is asnp
is mentioned by
dbSNPrs1064796203
dbSNP (classic)rs1064796203
ClinGenrs1064796203
ebirs1064796203
HLIrs1064796203
Exacrs1064796203
Gnomadrs1064796203
Varsomers1064796203
LitVarrs1064796203
Maprs1064796203
PheGenIrs1064796203
Biobankrs1064796203
1000 genomesrs1064796203
hgdprs1064796203
ensemblrs1064796203
geneviewrs1064796203
scholarrs1064796203
googlers1064796203
pharmgkbrs1064796203
gwascentralrs1064796203
openSNPrs1064796203
23andMers1064796203
23andMe allrs1064796203
SNPshotrs1064796203
SNPdbers1064796203
MSV3drs1064796203
GWAS Ctlgrs1064796203
Max Magnitude0
ClinVar
Risk rs1064796203(-;-)
Alt rs1064796203(-;-)
Reference Rs1064796203(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166211173delA
CLNSRC
CLNACC RCV000487276.1,