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rs796053010

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053010(C;C)
Make rs796053010(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165999748
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053010
ebirs796053010
HLIrs796053010
Exacrs796053010
Varsomers796053010
Maprs796053010
PheGenIrs796053010
hapmaprs796053010
1000 genomesrs796053010
hgdprs796053010
ensemblrs796053010
gopubmedrs796053010
geneviewrs796053010
scholarrs796053010
googlers796053010
pharmgkbrs796053010
gwascentralrs796053010
openSNPrs796053010
23andMers796053010
23andMe allrs796053010
SNP Nexus

SNPshotrs796053010
SNPdbers796053010
MSV3drs796053010
GWAS Ctlgrs796053010
Max Magnitude0
ClinVar
Risk rs796053010(C;C)
Alt rs796053010(C;C)
Reference rs796053010(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166856258A>G
CLNSRC
CLNACC RCV000188947.1,