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rs796053079

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053079(-;-)
Make rs796053079(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165999743
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053079
ebirs796053079
HLIrs796053079
Exacrs796053079
Varsomers796053079
Maprs796053079
PheGenIrs796053079
hapmaprs796053079
1000 genomesrs796053079
hgdprs796053079
ensemblrs796053079
gopubmedrs796053079
geneviewrs796053079
scholarrs796053079
googlers796053079
pharmgkbrs796053079
gwascentralrs796053079
openSNPrs796053079
23andMers796053079
23andMe allrs796053079
SNP Nexus

SNPshotrs796053079
SNPdbers796053079
MSV3drs796053079
GWAS Ctlgrs796053079
Max Magnitude0
ClinVar
Risk rs796053079(;)
Alt rs796053079(;)
Reference rs796053079(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166856253delC
CLNSRC
CLNACC RCV000189059.1,