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rs869312966

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312966(G;T)
Make rs869312966(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position51806345
GeneSCN8A
is asnp
is mentioned by
dbSNPrs869312966
ebirs869312966
HLIrs869312966
Exacrs869312966
Varsomers869312966
Maprs869312966
PheGenIrs869312966
hapmaprs869312966
1000 genomesrs869312966
hgdprs869312966
ensemblrs869312966
gopubmedrs869312966
geneviewrs869312966
scholarrs869312966
googlers869312966
pharmgkbrs869312966
gwascentralrs869312966
openSNPrs869312966
23andMers869312966
23andMe allrs869312966
SNP Nexus

SNPshotrs869312966
SNPdbers869312966
MSV3drs869312966
GWAS Ctlgrs869312966
Max Magnitude0
ClinVar
Risk rs869312966(T;T)
Alt rs869312966(T;T)
Reference rs869312966(G;G)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene SCN8A
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000012.11:g.52200129G>T
CLNSRC
CLNACC RCV000210663.1,