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rs796053081

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053081(-;-)
Make rs796053081(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165996046
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053081
ebirs796053081
HLIrs796053081
Exacrs796053081
Varsomers796053081
Maprs796053081
PheGenIrs796053081
hapmaprs796053081
1000 genomesrs796053081
hgdprs796053081
ensemblrs796053081
gopubmedrs796053081
geneviewrs796053081
scholarrs796053081
googlers796053081
pharmgkbrs796053081
gwascentralrs796053081
openSNPrs796053081
23andMers796053081
23andMe allrs796053081
SNP Nexus

SNPshotrs796053081
SNPdbers796053081
MSV3drs796053081
GWAS Ctlgrs796053081
Max Magnitude0
ClinVar
Risk rs796053081(;)
Alt rs796053081(;)
Reference rs796053081(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166852556delC
CLNSRC
CLNACC RCV000189061.1,