Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1057521223

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057521223(A;A)
Make rs1057521223(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position165373339
GeneSCN2A
is asnp
is mentioned by
dbSNPrs1057521223
dbSNP (old)rs1057521223
ClinGenrs1057521223
ebirs1057521223
HLIrs1057521223
Exacrs1057521223
Gnomadrs1057521223
Varsomers1057521223
Maprs1057521223
PheGenIrs1057521223
Biobankrs1057521223
1000 genomesrs1057521223
hgdprs1057521223
ensemblrs1057521223
gopubmedrs1057521223
geneviewrs1057521223
scholarrs1057521223
googlers1057521223
pharmgkbrs1057521223
gwascentralrs1057521223
openSNPrs1057521223
23andMers1057521223
23andMe allrs1057521223
SNPshotrs1057521223
SNPdbers1057521223
MSV3drs1057521223
GWAS Ctlgrs1057521223
Max Magnitude0
ClinVar
Risk rs1057521223(A;A)
Alt rs1057521223(A;A)
Reference Rs1057521223(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166229849G>A
CLNSRC
CLNACC RCV000440836.1,