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rs1057520361

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057520361(C;T)
Make rs1057520361(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position51687102
GeneSCN8A
is asnp
is mentioned by
dbSNPrs1057520361
dbSNP (old)rs1057520361
ClinGenrs1057520361
ebirs1057520361
HLIrs1057520361
Exacrs1057520361
Gnomadrs1057520361
Varsomers1057520361
Maprs1057520361
PheGenIrs1057520361
Biobankrs1057520361
1000 genomesrs1057520361
hgdprs1057520361
ensemblrs1057520361
gopubmedrs1057520361
geneviewrs1057520361
scholarrs1057520361
googlers1057520361
pharmgkbrs1057520361
gwascentralrs1057520361
openSNPrs1057520361
23andMers1057520361
23andMe allrs1057520361
SNPshotrs1057520361
SNPdbers1057520361
MSV3drs1057520361
GWAS Ctlgrs1057520361
Max Magnitude0
ClinVar
Risk rs1057520361(T;T)
Alt rs1057520361(T;T)
Reference Rs1057520361(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN8A
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52080886C>T
CLNSRC
CLNACC RCV000420545.1,