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rs796053078

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs796053078(-;-)
Make rs796053078(-;G)
Make rs796053078(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166002539
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053078
ebirs796053078
HLIrs796053078
Exacrs796053078
Varsomers796053078
Maprs796053078
PheGenIrs796053078
hapmaprs796053078
1000 genomesrs796053078
hgdprs796053078
ensemblrs796053078
gopubmedrs796053078
geneviewrs796053078
scholarrs796053078
googlers796053078
pharmgkbrs796053078
gwascentralrs796053078
openSNPrs796053078
23andMers796053078
23andMe allrs796053078
SNP Nexus

SNPshotrs796053078
SNPdbers796053078
MSV3drs796053078
GWAS Ctlgrs796053078
Max Magnitude0
ClinVar
Risk rs796053078(G;G)
Alt rs796053078(G;G)
Reference rs796053078(;)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166859050dupC
CLNSRC
CLNACC RCV000189058.1,