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rs796053068

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053068(-;-)
Make rs796053068(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166013896
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053068
ebirs796053068
HLIrs796053068
Exacrs796053068
Varsomers796053068
Maprs796053068
PheGenIrs796053068
hapmaprs796053068
1000 genomesrs796053068
hgdprs796053068
ensemblrs796053068
gopubmedrs796053068
geneviewrs796053068
scholarrs796053068
googlers796053068
pharmgkbrs796053068
gwascentralrs796053068
openSNPrs796053068
23andMers796053068
23andMe allrs796053068
SNP Nexus

SNPshotrs796053068
SNPdbers796053068
MSV3drs796053068
GWAS Ctlgrs796053068
Max Magnitude0
ClinVar
Risk rs796053068(;)
Alt rs796053068(;)
Reference rs796053068(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166870406delA
CLNSRC
CLNACC RCV000189048.1,