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rs796053043

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053043(C;T)
Make rs796053043(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165991655
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053043
ebirs796053043
HLIrs796053043
Exacrs796053043
Varsomers796053043
Maprs796053043
PheGenIrs796053043
hapmaprs796053043
1000 genomesrs796053043
hgdprs796053043
ensemblrs796053043
gopubmedrs796053043
geneviewrs796053043
scholarrs796053043
googlers796053043
pharmgkbrs796053043
gwascentralrs796053043
openSNPrs796053043
23andMers796053043
23andMe allrs796053043
SNP Nexus

SNPshotrs796053043
SNPdbers796053043
MSV3drs796053043
GWAS Ctlgrs796053043
Max Magnitude0
ClinVar
Risk rs796053043(T;T)
Alt rs796053043(T;T)
Reference rs796053043(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848165G>A
CLNSRC
CLNACC RCV000189011.1,