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rs796053214

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053214(G;T)
Make rs796053214(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position51786554
GeneSCN8A
is asnp
is mentioned by
dbSNPrs796053214
ebirs796053214
HLIrs796053214
Exacrs796053214
Varsomers796053214
Maprs796053214
PheGenIrs796053214
hapmaprs796053214
1000 genomesrs796053214
hgdprs796053214
ensemblrs796053214
gopubmedrs796053214
geneviewrs796053214
scholarrs796053214
googlers796053214
pharmgkbrs796053214
gwascentralrs796053214
openSNPrs796053214
23andMers796053214
23andMe allrs796053214
SNP Nexus

SNPshotrs796053214
SNPdbers796053214
MSV3drs796053214
GWAS Ctlgrs796053214
Max Magnitude0
ClinVar
Risk rs796053214(T;T)
Alt rs796053214(T;T)
Reference rs796053214(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN8A
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52180338G>T
CLNSRC
CLNACC RCV000189275.2,