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rs1057518356

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057518356(C;C)
Make rs1057518356(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position51762665
GeneSCN8A
is asnp
is mentioned by
dbSNPrs1057518356
dbSNP (old)rs1057518356
ClinGenrs1057518356
ebirs1057518356
HLIrs1057518356
Exacrs1057518356
Gnomadrs1057518356
Varsomers1057518356
Maprs1057518356
PheGenIrs1057518356
Biobankrs1057518356
1000 genomesrs1057518356
hgdprs1057518356
ensemblrs1057518356
gopubmedrs1057518356
geneviewrs1057518356
scholarrs1057518356
googlers1057518356
pharmgkbrs1057518356
gwascentralrs1057518356
openSNPrs1057518356
23andMers1057518356
23andMe allrs1057518356
SNPshotrs1057518356
SNPdbers1057518356
MSV3drs1057518356
GWAS Ctlgrs1057518356
Max Magnitude0
ClinVar
Risk rs1057518356(C;C)
Alt rs1057518356(C;C)
Reference Rs1057518356(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN8A
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52156449T>C
CLNSRC
CLNACC RCV000413870.1,