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rs796053007

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796053007(A;G)
Make rs796053007(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165999780
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053007
ebirs796053007
HLIrs796053007
Exacrs796053007
Varsomers796053007
Maprs796053007
PheGenIrs796053007
hapmaprs796053007
1000 genomesrs796053007
hgdprs796053007
ensemblrs796053007
gopubmedrs796053007
geneviewrs796053007
scholarrs796053007
googlers796053007
pharmgkbrs796053007
gwascentralrs796053007
openSNPrs796053007
23andMers796053007
23andMe allrs796053007
SNP Nexus

SNPshotrs796053007
SNPdbers796053007
MSV3drs796053007
GWAS Ctlgrs796053007
Max Magnitude0
ClinVar
Risk rs796053007(G;G)
Alt rs796053007(G;G)
Reference rs796053007(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166856290T>C
CLNSRC
CLNACC RCV000188944.2,