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rs796053040

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053040(A;A)
Make rs796053040(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165991840
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053040
ebirs796053040
HLIrs796053040
Exacrs796053040
Varsomers796053040
Maprs796053040
PheGenIrs796053040
hapmaprs796053040
1000 genomesrs796053040
hgdprs796053040
ensemblrs796053040
gopubmedrs796053040
geneviewrs796053040
scholarrs796053040
googlers796053040
pharmgkbrs796053040
gwascentralrs796053040
openSNPrs796053040
23andMers796053040
23andMe allrs796053040
SNP Nexus

SNPshotrs796053040
SNPdbers796053040
MSV3drs796053040
GWAS Ctlgrs796053040
Max Magnitude0
ClinVar
Risk rs796053040(A;A)
Alt rs796053040(A;A)
Reference rs796053040(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848350C>T
CLNSRC
CLNACC RCV000189003.1,