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rs1057523696

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057523696(C;C)
Make rs1057523696(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position165344867
GeneSCN2A
is asnp
is mentioned by
dbSNPrs1057523696
dbSNP (old)rs1057523696
ClinGenrs1057523696
ebirs1057523696
HLIrs1057523696
Exacrs1057523696
Gnomadrs1057523696
Varsomers1057523696
LitVarrs1057523696
Maprs1057523696
PheGenIrs1057523696
Biobankrs1057523696
1000 genomesrs1057523696
hgdprs1057523696
ensemblrs1057523696
gopubmedrs1057523696
geneviewrs1057523696
scholarrs1057523696
googlers1057523696
pharmgkbrs1057523696
gwascentralrs1057523696
openSNPrs1057523696
23andMers1057523696
23andMe allrs1057523696
SNPshotrs1057523696
SNPdbers1057523696
MSV3drs1057523696
GWAS Ctlgrs1057523696
Max Magnitude0
ClinVar
Risk rs1057523696(C;C)
Alt rs1057523696(C;C)
Reference Rs1057523696(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166201377T>C
CLNSRC
CLNACC RCV000422689.1,