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rs796053090

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053090(C;C)
Make rs796053090(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166056412
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796053090
ebirs796053090
HLIrs796053090
Exacrs796053090
Varsomers796053090
Maprs796053090
PheGenIrs796053090
hapmaprs796053090
1000 genomesrs796053090
hgdprs796053090
ensemblrs796053090
gopubmedrs796053090
geneviewrs796053090
scholarrs796053090
googlers796053090
pharmgkbrs796053090
gwascentralrs796053090
openSNPrs796053090
23andMers796053090
23andMe allrs796053090
SNP Nexus

SNPshotrs796053090
SNPdbers796053090
MSV3drs796053090
GWAS Ctlgrs796053090
Max Magnitude0
ClinVar
Risk rs796053090(C;C)
Alt rs796053090(C;C)
Reference rs796053090(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166912922C>G
CLNSRC
CLNACC RCV000189072.2,