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rs796053050

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053050(-;-)
Make rs796053050(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166058661
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796053050
ebirs796053050
HLIrs796053050
Exacrs796053050
Varsomers796053050
Maprs796053050
PheGenIrs796053050
hapmaprs796053050
1000 genomesrs796053050
hgdprs796053050
ensemblrs796053050
gopubmedrs796053050
geneviewrs796053050
scholarrs796053050
googlers796053050
pharmgkbrs796053050
gwascentralrs796053050
openSNPrs796053050
23andMers796053050
23andMe allrs796053050
SNP Nexus

SNPshotrs796053050
SNPdbers796053050
MSV3drs796053050
GWAS Ctlgrs796053050
Max Magnitude0
ClinVar
Risk rs796053050(;)
Alt rs796053050(;)
Reference rs796053050(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166915171delC
CLNSRC
CLNACC RCV000189030.1,