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rs1064796620

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome2
Position165388809
GeneSCN2A
is asnp
is mentioned by
dbSNPrs1064796620
dbSNP (old)rs1064796620
ClinGenrs1064796620
ebirs1064796620
HLIrs1064796620
Exacrs1064796620
Gnomadrs1064796620
Varsomers1064796620
Maprs1064796620
PheGenIrs1064796620
Biobankrs1064796620
1000 genomesrs1064796620
hgdprs1064796620
ensemblrs1064796620
gopubmedrs1064796620
geneviewrs1064796620
scholarrs1064796620
googlers1064796620
pharmgkbrs1064796620
gwascentralrs1064796620
openSNPrs1064796620
23andMers1064796620
23andMe allrs1064796620
SNPshotrs1064796620
SNPdbers1064796620
MSV3drs1064796620
GWAS Ctlgrs1064796620
Max Magnitude0
ClinVar
Risk rs1064796620(-;-)
Alt rs1064796620(-;-)
Reference Rs1064796620(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166245319delT
CLNSRC
CLNACC RCV000486948.1,