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rs796053026

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053026(G;G)
Make rs796053026(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165994204
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053026
ebirs796053026
HLIrs796053026
Exacrs796053026
Varsomers796053026
Maprs796053026
PheGenIrs796053026
hapmaprs796053026
1000 genomesrs796053026
hgdprs796053026
ensemblrs796053026
gopubmedrs796053026
geneviewrs796053026
scholarrs796053026
googlers796053026
pharmgkbrs796053026
gwascentralrs796053026
openSNPrs796053026
23andMers796053026
23andMe allrs796053026
SNP Nexus

SNPshotrs796053026
SNPdbers796053026
MSV3drs796053026
GWAS Ctlgrs796053026
Max Magnitude0
ClinVar
Risk rs796053026(G;G)
Alt rs796053026(G;G)
Reference rs796053026(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166850714A>C
CLNSRC
CLNACC RCV000188975.1,