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rs796053057

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053057(-;-)
Make rs796053057(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166045275
GeneSCN1A
is asnp
is mentioned by
dbSNPrs796053057
ebirs796053057
HLIrs796053057
Exacrs796053057
Varsomers796053057
Maprs796053057
PheGenIrs796053057
hapmaprs796053057
1000 genomesrs796053057
hgdprs796053057
ensemblrs796053057
gopubmedrs796053057
geneviewrs796053057
scholarrs796053057
googlers796053057
pharmgkbrs796053057
gwascentralrs796053057
openSNPrs796053057
23andMers796053057
23andMe allrs796053057
SNP Nexus

SNPshotrs796053057
SNPdbers796053057
MSV3drs796053057
GWAS Ctlgrs796053057
Max Magnitude0
ClinVar
Risk rs796053057(;)
Alt rs796053057(;)
Reference rs796053057(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166901785delC
CLNSRC
CLNACC RCV000189037.1,