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rs796053224

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053224(C;T)
Make rs796053224(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position51806435
GeneSCN8A
is asnp
is mentioned by
dbSNPrs796053224
ebirs796053224
HLIrs796053224
Exacrs796053224
Varsomers796053224
Maprs796053224
PheGenIrs796053224
hapmaprs796053224
1000 genomesrs796053224
hgdprs796053224
ensemblrs796053224
gopubmedrs796053224
geneviewrs796053224
scholarrs796053224
googlers796053224
pharmgkbrs796053224
gwascentralrs796053224
openSNPrs796053224
23andMers796053224
23andMe allrs796053224
SNP Nexus

SNPshotrs796053224
SNPdbers796053224
MSV3drs796053224
GWAS Ctlgrs796053224
Max Magnitude0
ClinVar
Risk rs796053224(T;T)
Alt rs796053224(T;T)
Reference rs796053224(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN8A
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52200219C>T
CLNSRC
CLNACC RCV000189285.2,