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rs1064795014

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome2
Position165310343
GeneSCN2A
is asnp
is mentioned by
dbSNPrs1064795014
dbSNP (old)rs1064795014
ClinGenrs1064795014
ebirs1064795014
HLIrs1064795014
Exacrs1064795014
Gnomadrs1064795014
Varsomers1064795014
Maprs1064795014
PheGenIrs1064795014
Biobankrs1064795014
1000 genomesrs1064795014
hgdprs1064795014
ensemblrs1064795014
gopubmedrs1064795014
geneviewrs1064795014
scholarrs1064795014
googlers1064795014
pharmgkbrs1064795014
gwascentralrs1064795014
openSNPrs1064795014
23andMers1064795014
23andMe allrs1064795014
SNPshotrs1064795014
SNPdbers1064795014
MSV3drs1064795014
GWAS Ctlgrs1064795014
Max Magnitude0
ClinVar
Risk rs1064795014(A;A)
Alt rs1064795014(A;A)
Reference Rs1064795014(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166166853G>A
CLNSRC
CLNACC RCV000479851.1,