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rs1057524820

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057524820(G;T)
Make rs1057524820(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position51765746
GeneSCN8A
is asnp
is mentioned by
dbSNPrs1057524820
dbSNP (old)rs1057524820
ClinGenrs1057524820
ebirs1057524820
HLIrs1057524820
Exacrs1057524820
Gnomadrs1057524820
Varsomers1057524820
Maprs1057524820
PheGenIrs1057524820
Biobankrs1057524820
1000 genomesrs1057524820
hgdprs1057524820
ensemblrs1057524820
gopubmedrs1057524820
geneviewrs1057524820
scholarrs1057524820
googlers1057524820
pharmgkbrs1057524820
gwascentralrs1057524820
openSNPrs1057524820
23andMers1057524820
23andMe allrs1057524820
SNPshotrs1057524820
SNPdbers1057524820
MSV3drs1057524820
GWAS Ctlgrs1057524820
Max Magnitude0
ClinVar
Risk rs1057524820(T;T)
Alt rs1057524820(T;T)
Reference Rs1057524820(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN8A
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52159530G>T
CLNSRC
CLNACC RCV000425333.1,