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rs796053033

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053033(A;A)
Make rs796053033(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165992154
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053033
ebirs796053033
HLIrs796053033
Exacrs796053033
Varsomers796053033
Maprs796053033
PheGenIrs796053033
hapmaprs796053033
1000 genomesrs796053033
hgdprs796053033
ensemblrs796053033
gopubmedrs796053033
geneviewrs796053033
scholarrs796053033
googlers796053033
pharmgkbrs796053033
gwascentralrs796053033
openSNPrs796053033
23andMers796053033
23andMe allrs796053033
SNP Nexus

SNPshotrs796053033
SNPdbers796053033
MSV3drs796053033
GWAS Ctlgrs796053033
Max Magnitude0
ClinVar
Risk rs796053033(A;A)
Alt rs796053033(A;A)
Reference rs796053033(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848664A>T
CLNSRC
CLNACC RCV000188992.1,