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rs796053036

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053036(G;T)
Make rs796053036(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165992014
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053036
ebirs796053036
HLIrs796053036
Exacrs796053036
Varsomers796053036
Maprs796053036
PheGenIrs796053036
hapmaprs796053036
1000 genomesrs796053036
hgdprs796053036
ensemblrs796053036
gopubmedrs796053036
geneviewrs796053036
scholarrs796053036
googlers796053036
pharmgkbrs796053036
gwascentralrs796053036
openSNPrs796053036
23andMers796053036
23andMe allrs796053036
SNP Nexus

SNPshotrs796053036
SNPdbers796053036
MSV3drs796053036
GWAS Ctlgrs796053036
Max Magnitude0
ClinVar
Risk rs796053036(T;T)
Alt rs796053036(T;T)
Reference rs796053036(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848524C>A
CLNSRC
CLNACC RCV000188997.2,