Have questions? Visit https://www.reddit.com/r/SNPedia

rs796053028

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053028(A;A)
Make rs796053028(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165994217
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053028
ebirs796053028
HLIrs796053028
Exacrs796053028
Varsomers796053028
Maprs796053028
PheGenIrs796053028
hapmaprs796053028
1000 genomesrs796053028
hgdprs796053028
ensemblrs796053028
gopubmedrs796053028
geneviewrs796053028
scholarrs796053028
googlers796053028
pharmgkbrs796053028
gwascentralrs796053028
openSNPrs796053028
23andMers796053028
23andMe allrs796053028
SNP Nexus

SNPshotrs796053028
SNPdbers796053028
MSV3drs796053028
GWAS Ctlgrs796053028
Max Magnitude0
ClinVar
Risk rs796053028(A;A)
Alt rs796053028(A;A)
Reference rs796053028(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166850727G>T
CLNSRC
CLNACC RCV000188977.1,