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rs796053106

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs796053106(-;-)
Make rs796053106(-;T)
Make rs796053106(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166047743
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796053106
ebirs796053106
HLIrs796053106
Exacrs796053106
Varsomers796053106
Maprs796053106
PheGenIrs796053106
hapmaprs796053106
1000 genomesrs796053106
hgdprs796053106
ensemblrs796053106
gopubmedrs796053106
geneviewrs796053106
scholarrs796053106
googlers796053106
pharmgkbrs796053106
gwascentralrs796053106
openSNPrs796053106
23andMers796053106
23andMe allrs796053106
SNP Nexus

SNPshotrs796053106
SNPdbers796053106
MSV3drs796053106
GWAS Ctlgrs796053106
Max Magnitude0
ClinVar
Risk rs796053106(T;T)
Alt rs796053106(T;T)
Reference rs796053106(;)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166904254dupA
CLNSRC
CLNACC RCV000189098.1,