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rs748333147

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs748333147(C;T)
Make rs748333147(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position165992171
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs748333147
ebirs748333147
HLIrs748333147
Exacrs748333147
Varsomers748333147
Maprs748333147
PheGenIrs748333147
hapmaprs748333147
1000 genomesrs748333147
hgdprs748333147
ensemblrs748333147
gopubmedrs748333147
geneviewrs748333147
scholarrs748333147
googlers748333147
pharmgkbrs748333147
gwascentralrs748333147
openSNPrs748333147
23andMers748333147
23andMe allrs748333147
SNP Nexus

SNPshotrs748333147
SNPdbers748333147
MSV3drs748333147
GWAS Ctlgrs748333147
Max Magnitude0
ClinVar
Risk rs748333147(A,T;A,T)
Alt rs748333147(A,T;A,T)
Reference rs748333147(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166848681C>A
CLNSRC
CLNACC RCV000188991.1,