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rs796053029

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053029(C;C)
Make rs796053029(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165992359
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053029
ebirs796053029
HLIrs796053029
Exacrs796053029
Varsomers796053029
Maprs796053029
PheGenIrs796053029
hapmaprs796053029
1000 genomesrs796053029
hgdprs796053029
ensemblrs796053029
gopubmedrs796053029
geneviewrs796053029
scholarrs796053029
googlers796053029
pharmgkbrs796053029
gwascentralrs796053029
openSNPrs796053029
23andMers796053029
23andMe allrs796053029
SNP Nexus

SNPshotrs796053029
SNPdbers796053029
MSV3drs796053029
GWAS Ctlgrs796053029
Max Magnitude0
ClinVar
Risk rs796053029(C;C)
Alt rs796053029(C;C)
Reference rs796053029(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848869C>G
CLNSRC
CLNACC RCV000188984.2,