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rs1057523734

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057523734(A;A)
Make rs1057523734(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position165374869
GeneSCN2A
is asnp
is mentioned by
dbSNPrs1057523734
dbSNP (old)rs1057523734
ClinGenrs1057523734
ebirs1057523734
HLIrs1057523734
Exacrs1057523734
Gnomadrs1057523734
Varsomers1057523734
LitVarrs1057523734
Maprs1057523734
PheGenIrs1057523734
Biobankrs1057523734
1000 genomesrs1057523734
hgdprs1057523734
ensemblrs1057523734
gopubmedrs1057523734
geneviewrs1057523734
scholarrs1057523734
googlers1057523734
pharmgkbrs1057523734
gwascentralrs1057523734
openSNPrs1057523734
23andMers1057523734
23andMe allrs1057523734
SNPshotrs1057523734
SNPdbers1057523734
MSV3drs1057523734
GWAS Ctlgrs1057523734
Max Magnitude0
ClinVar
Risk rs1057523734(A;A)
Alt rs1057523734(A;A)
Reference Rs1057523734(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166231379G>A
CLNSRC
CLNACC RCV000422482.1,