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rs796052969

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052969(A;G)
Make rs796052969(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166048919
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796052969
ebirs796052969
HLIrs796052969
Exacrs796052969
Varsomers796052969
Maprs796052969
PheGenIrs796052969
hapmaprs796052969
1000 genomesrs796052969
hgdprs796052969
ensemblrs796052969
gopubmedrs796052969
geneviewrs796052969
scholarrs796052969
googlers796052969
pharmgkbrs796052969
gwascentralrs796052969
openSNPrs796052969
23andMers796052969
23andMe allrs796052969
SNP Nexus

SNPshotrs796052969
SNPdbers796052969
MSV3drs796052969
GWAS Ctlgrs796052969
Max Magnitude0
ClinVar
Risk rs796052969(G;G)
Alt rs796052969(G;G)
Reference rs796052969(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166905429T>C
CLNSRC
CLNACC RCV000188857.2,