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rs796053024

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053024(G;T)
Make rs796053024(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165994317
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053024
ebirs796053024
HLIrs796053024
Exacrs796053024
Varsomers796053024
Maprs796053024
PheGenIrs796053024
hapmaprs796053024
1000 genomesrs796053024
hgdprs796053024
ensemblrs796053024
gopubmedrs796053024
geneviewrs796053024
scholarrs796053024
googlers796053024
pharmgkbrs796053024
gwascentralrs796053024
openSNPrs796053024
23andMers796053024
23andMe allrs796053024
SNP Nexus

SNPshotrs796053024
SNPdbers796053024
MSV3drs796053024
GWAS Ctlgrs796053024
Max Magnitude0
ClinVar
Risk rs796053024(T;T)
Alt rs796053024(T;T)
Reference rs796053024(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166850827C>A
CLNSRC
CLNACC RCV000188970.1,