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rs796053044

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053044(C;C)
Make rs796053044(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165991648
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053044
ebirs796053044
HLIrs796053044
Exacrs796053044
Varsomers796053044
Maprs796053044
PheGenIrs796053044
hapmaprs796053044
1000 genomesrs796053044
hgdprs796053044
ensemblrs796053044
gopubmedrs796053044
geneviewrs796053044
scholarrs796053044
googlers796053044
pharmgkbrs796053044
gwascentralrs796053044
openSNPrs796053044
23andMers796053044
23andMe allrs796053044
SNP Nexus

SNPshotrs796053044
SNPdbers796053044
MSV3drs796053044
GWAS Ctlgrs796053044
Max Magnitude0
ClinVar
Risk rs796053044(C;C)
Alt rs796053044(C;C)
Reference rs796053044(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848158A>G
CLNSRC
CLNACC RCV000189012.1,