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rs796053009

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053009(G;G)
Make rs796053009(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165999757
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053009
ebirs796053009
HLIrs796053009
Exacrs796053009
Varsomers796053009
Maprs796053009
PheGenIrs796053009
hapmaprs796053009
1000 genomesrs796053009
hgdprs796053009
ensemblrs796053009
gopubmedrs796053009
geneviewrs796053009
scholarrs796053009
googlers796053009
pharmgkbrs796053009
gwascentralrs796053009
openSNPrs796053009
23andMers796053009
23andMe allrs796053009
SNP Nexus

SNPshotrs796053009
SNPdbers796053009
MSV3drs796053009
GWAS Ctlgrs796053009
Max Magnitude0
ClinVar
Risk rs796053009(G;G)
Alt rs796053009(G;G)
Reference rs796053009(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166856267A>C
CLNSRC
CLNACC RCV000188946.1,