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rs796053071

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053071(-;-)
Make rs796053071(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166036068
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053071
ebirs796053071
HLIrs796053071
Exacrs796053071
Varsomers796053071
Maprs796053071
PheGenIrs796053071
hapmaprs796053071
1000 genomesrs796053071
hgdprs796053071
ensemblrs796053071
gopubmedrs796053071
geneviewrs796053071
scholarrs796053071
googlers796053071
pharmgkbrs796053071
gwascentralrs796053071
openSNPrs796053071
23andMers796053071
23andMe allrs796053071
SNP Nexus

SNPshotrs796053071
SNPdbers796053071
MSV3drs796053071
GWAS Ctlgrs796053071
Max Magnitude0
ClinVar
Risk rs796053071(;)
Alt rs796053071(;)
Reference rs796053071(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166892578delC
CLNSRC
CLNACC RCV000189051.1,