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rs796052965

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052965(A;A)
Make rs796052965(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166051714
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796052965
ebirs796052965
HLIrs796052965
Exacrs796052965
Varsomers796052965
Maprs796052965
PheGenIrs796052965
hapmaprs796052965
1000 genomesrs796052965
hgdprs796052965
ensemblrs796052965
gopubmedrs796052965
geneviewrs796052965
scholarrs796052965
googlers796052965
pharmgkbrs796052965
gwascentralrs796052965
openSNPrs796052965
23andMers796052965
23andMe allrs796052965
SNP Nexus

SNPshotrs796052965
SNPdbers796052965
MSV3drs796052965
GWAS Ctlgrs796052965
Max Magnitude0
ClinVar
Risk rs796052965(A;A)
Alt rs796052965(A;A)
Reference rs796052965(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166908224C>T
CLNSRC
CLNACC RCV000188850.2,