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rs796053035

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053035(A;A)
Make rs796053035(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165992057
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053035
ebirs796053035
HLIrs796053035
Exacrs796053035
Varsomers796053035
Maprs796053035
PheGenIrs796053035
hapmaprs796053035
1000 genomesrs796053035
hgdprs796053035
ensemblrs796053035
gopubmedrs796053035
geneviewrs796053035
scholarrs796053035
googlers796053035
pharmgkbrs796053035
gwascentralrs796053035
openSNPrs796053035
23andMers796053035
23andMe allrs796053035
SNP Nexus

SNPshotrs796053035
SNPdbers796053035
MSV3drs796053035
GWAS Ctlgrs796053035
Max Magnitude0
ClinVar
Risk rs796053035(A;A)
Alt rs796053035(A;A)
Reference rs796053035(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848567C>T
CLNSRC
CLNACC RCV000188995.1,