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rs796053059

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs796053059(-;-)
Make rs796053059(-;G)
Make rs796053059(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166045167
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796053059
ebirs796053059
HLIrs796053059
Exacrs796053059
Varsomers796053059
Maprs796053059
PheGenIrs796053059
hapmaprs796053059
1000 genomesrs796053059
hgdprs796053059
ensemblrs796053059
gopubmedrs796053059
geneviewrs796053059
scholarrs796053059
googlers796053059
pharmgkbrs796053059
gwascentralrs796053059
openSNPrs796053059
23andMers796053059
23andMe allrs796053059
SNP Nexus

SNPshotrs796053059
SNPdbers796053059
MSV3drs796053059
GWAS Ctlgrs796053059
Max Magnitude0
ClinVar
Risk rs796053059(G;G)
Alt rs796053059(G;G)
Reference rs796053059(;)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166901678dupC
CLNSRC
CLNACC RCV000189039.1,