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rs796053042

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053042(C;C)
Make rs796053042(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165991693
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053042
ebirs796053042
HLIrs796053042
Exacrs796053042
Varsomers796053042
Maprs796053042
PheGenIrs796053042
hapmaprs796053042
1000 genomesrs796053042
hgdprs796053042
ensemblrs796053042
gopubmedrs796053042
geneviewrs796053042
scholarrs796053042
googlers796053042
pharmgkbrs796053042
gwascentralrs796053042
openSNPrs796053042
23andMers796053042
23andMe allrs796053042
SNP Nexus

SNPshotrs796053042
SNPdbers796053042
MSV3drs796053042
GWAS Ctlgrs796053042
Max Magnitude0
ClinVar
Risk rs796053042(C;C)
Alt rs796053042(C;C)
Reference rs796053042(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848203C>G
CLNSRC
CLNACC RCV000189010.1,