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rs1064794721

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome2
Position165388770
GeneSCN2A
is asnp
is mentioned by
dbSNPrs1064794721
dbSNP (classic)rs1064794721
ClinGenrs1064794721
ebirs1064794721
HLIrs1064794721
Exacrs1064794721
Gnomadrs1064794721
Varsomers1064794721
LitVarrs1064794721
Maprs1064794721
PheGenIrs1064794721
Biobankrs1064794721
1000 genomesrs1064794721
hgdprs1064794721
ensemblrs1064794721
geneviewrs1064794721
scholarrs1064794721
googlers1064794721
pharmgkbrs1064794721
gwascentralrs1064794721
openSNPrs1064794721
23andMers1064794721
SNPshotrs1064794721
SNPdbers1064794721
MSV3drs1064794721
GWAS Ctlgrs1064794721
Max Magnitude0
ClinVar
Risk rs1064794721(C;C)
Alt rs1064794721(C;C)
Reference Rs1064794721(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166245280T>C
CLNSRC
CLNACC RCV000480069.1,