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rs796053065

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053065(-;-)
Make rs796053065(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166039443
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796053065
ebirs796053065
HLIrs796053065
Exacrs796053065
Varsomers796053065
Maprs796053065
PheGenIrs796053065
hapmaprs796053065
1000 genomesrs796053065
hgdprs796053065
ensemblrs796053065
gopubmedrs796053065
geneviewrs796053065
scholarrs796053065
googlers796053065
pharmgkbrs796053065
gwascentralrs796053065
openSNPrs796053065
23andMers796053065
23andMe allrs796053065
SNP Nexus

SNPshotrs796053065
SNPdbers796053065
MSV3drs796053065
GWAS Ctlgrs796053065
Max Magnitude0
ClinVar
Risk rs796053065(;)
Alt rs796053065(;)
Reference rs796053065(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166895953delC
CLNSRC
CLNACC RCV000189045.1,