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rs1057520413

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520413(A;A)
Make rs1057520413(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position165310406
GeneSCN2A
is asnp
is mentioned by
dbSNPrs1057520413
dbSNP (old)rs1057520413
ClinGenrs1057520413
ebirs1057520413
HLIrs1057520413
Exacrs1057520413
Gnomadrs1057520413
Varsomers1057520413
LitVarrs1057520413
Maprs1057520413
PheGenIrs1057520413
Biobankrs1057520413
1000 genomesrs1057520413
hgdprs1057520413
ensemblrs1057520413
gopubmedrs1057520413
geneviewrs1057520413
scholarrs1057520413
googlers1057520413
pharmgkbrs1057520413
gwascentralrs1057520413
openSNPrs1057520413
23andMers1057520413
23andMe allrs1057520413
SNPshotrs1057520413
SNPdbers1057520413
MSV3drs1057520413
GWAS Ctlgrs1057520413
Max Magnitude0
ClinVar
Risk rs1057520413(A;A)
Alt rs1057520413(A;A)
Reference Rs1057520413(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166166916G>A
CLNSRC
CLNACC RCV000436956.1,