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rs1064795832

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome2
Position165367339
GeneSCN2A
is asnp
is mentioned by
dbSNPrs1064795832
dbSNP (old)rs1064795832
ClinGenrs1064795832
ebirs1064795832
HLIrs1064795832
Exacrs1064795832
Gnomadrs1064795832
Varsomers1064795832
Maprs1064795832
PheGenIrs1064795832
Biobankrs1064795832
1000 genomesrs1064795832
hgdprs1064795832
ensemblrs1064795832
gopubmedrs1064795832
geneviewrs1064795832
scholarrs1064795832
googlers1064795832
pharmgkbrs1064795832
gwascentralrs1064795832
openSNPrs1064795832
23andMers1064795832
23andMe allrs1064795832
SNPshotrs1064795832
SNPdbers1064795832
MSV3drs1064795832
GWAS Ctlgrs1064795832
Max Magnitude0
ClinVar
Risk rs1064795832(T;T)
Alt rs1064795832(T;T)
Reference Rs1064795832(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166223849G>T
CLNSRC
CLNACC RCV000479012.1,