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rs1057519210

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519210(C;T)
Make rs1057519210(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position51705423
GeneSCN8A
is asnp
is mentioned by
dbSNPrs1057519210
dbSNP (old)rs1057519210
ClinGenrs1057519210
ebirs1057519210
HLIrs1057519210
Exacrs1057519210
Gnomadrs1057519210
Varsomers1057519210
Maprs1057519210
PheGenIrs1057519210
Biobankrs1057519210
1000 genomesrs1057519210
hgdprs1057519210
ensemblrs1057519210
gopubmedrs1057519210
geneviewrs1057519210
scholarrs1057519210
googlers1057519210
pharmgkbrs1057519210
gwascentralrs1057519210
openSNPrs1057519210
23andMers1057519210
23andMe allrs1057519210
SNPshotrs1057519210
SNPdbers1057519210
MSV3drs1057519210
GWAS Ctlgrs1057519210
Max Magnitude0
ClinVar
Risk rs1057519210(T;T)
Alt rs1057519210(T;T)
Reference Rs1057519210(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN8A
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52099207C>T
CLNSRC
CLNACC RCV000416108.1,