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rs1057523786

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057523786(A;G)
Make rs1057523786(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position165354262
GeneSCN2A
is asnp
is mentioned by
dbSNPrs1057523786
dbSNP (old)rs1057523786
ClinGenrs1057523786
ebirs1057523786
HLIrs1057523786
Exacrs1057523786
Gnomadrs1057523786
Varsomers1057523786
Maprs1057523786
PheGenIrs1057523786
Biobankrs1057523786
1000 genomesrs1057523786
hgdprs1057523786
ensemblrs1057523786
gopubmedrs1057523786
geneviewrs1057523786
scholarrs1057523786
googlers1057523786
pharmgkbrs1057523786
gwascentralrs1057523786
openSNPrs1057523786
23andMers1057523786
23andMe allrs1057523786
SNPshotrs1057523786
SNPdbers1057523786
MSV3drs1057523786
GWAS Ctlgrs1057523786
Max Magnitude0
ClinVar
Risk rs1057523786(G;G)
Alt rs1057523786(G;G)
Reference Rs1057523786(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166210772A>G
CLNSRC
CLNACC RCV000438096.1,