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rs796053064

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053064(-;-)
Make rs796053064(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166043860
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796053064
ebirs796053064
HLIrs796053064
Exacrs796053064
Varsomers796053064
Maprs796053064
PheGenIrs796053064
hapmaprs796053064
1000 genomesrs796053064
hgdprs796053064
ensemblrs796053064
gopubmedrs796053064
geneviewrs796053064
scholarrs796053064
googlers796053064
pharmgkbrs796053064
gwascentralrs796053064
openSNPrs796053064
23andMers796053064
23andMe allrs796053064
SNP Nexus

SNPshotrs796053064
SNPdbers796053064
MSV3drs796053064
GWAS Ctlgrs796053064
Max Magnitude0
ClinVar
Risk rs796053064(;)
Alt rs796053064(;)
Reference rs796053064(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166900370delG
CLNSRC
CLNACC RCV000189044.1,