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rs796053084

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs796053084(-;-)
Make rs796053084(-;T)
Make rs796053084(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165992378
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053084
ebirs796053084
HLIrs796053084
Exacrs796053084
Varsomers796053084
Maprs796053084
PheGenIrs796053084
hapmaprs796053084
1000 genomesrs796053084
hgdprs796053084
ensemblrs796053084
gopubmedrs796053084
geneviewrs796053084
scholarrs796053084
googlers796053084
pharmgkbrs796053084
gwascentralrs796053084
openSNPrs796053084
23andMers796053084
23andMe allrs796053084
SNP Nexus

SNPshotrs796053084
SNPdbers796053084
MSV3drs796053084
GWAS Ctlgrs796053084
Max Magnitude0
ClinVar
Risk rs796053084(T;T)
Alt rs796053084(T;T)
Reference rs796053084(;)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848889dupA
CLNSRC
CLNACC RCV000189064.1,