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rs796053087

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053087(-;-)
Make rs796053087(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165991529
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053087
ebirs796053087
HLIrs796053087
Exacrs796053087
Varsomers796053087
Maprs796053087
PheGenIrs796053087
hapmaprs796053087
1000 genomesrs796053087
hgdprs796053087
ensemblrs796053087
gopubmedrs796053087
geneviewrs796053087
scholarrs796053087
googlers796053087
pharmgkbrs796053087
gwascentralrs796053087
openSNPrs796053087
23andMers796053087
23andMe allrs796053087
SNP Nexus

SNPshotrs796053087
SNPdbers796053087
MSV3drs796053087
GWAS Ctlgrs796053087
Max Magnitude0
ClinVar
Risk rs796053087(;)
Alt rs796053087(;)
Reference rs796053087(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848039delC
CLNSRC
CLNACC RCV000189069.1,