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rs796053041

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053041(A;A)
Make rs796053041(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165991708
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053041
ebirs796053041
HLIrs796053041
Exacrs796053041
Varsomers796053041
Maprs796053041
PheGenIrs796053041
hapmaprs796053041
1000 genomesrs796053041
hgdprs796053041
ensemblrs796053041
gopubmedrs796053041
geneviewrs796053041
scholarrs796053041
googlers796053041
pharmgkbrs796053041
gwascentralrs796053041
openSNPrs796053041
23andMers796053041
23andMe allrs796053041
SNP Nexus

SNPshotrs796053041
SNPdbers796053041
MSV3drs796053041
GWAS Ctlgrs796053041
Max Magnitude0
ClinVar
Risk rs796053041(A,C;A,C)
Alt rs796053041(A,C;A,C)
Reference rs796053041(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848218A>G; NC_000002.11:g.166848218A>T
CLNSRC
CLNACC RCV000189008.2, RCV000189007.1,