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

rs796053025

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796053025(A;G)
Make rs796053025(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165994297
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796053025
ebirs796053025
HLIrs796053025
Exacrs796053025
Varsomers796053025
Maprs796053025
PheGenIrs796053025
hapmaprs796053025
1000 genomesrs796053025
hgdprs796053025
ensemblrs796053025
gopubmedrs796053025
geneviewrs796053025
scholarrs796053025
googlers796053025
pharmgkbrs796053025
gwascentralrs796053025
openSNPrs796053025
23andMers796053025
23andMe allrs796053025
SNP Nexus

SNPshotrs796053025
SNPdbers796053025
MSV3drs796053025
GWAS Ctlgrs796053025
Max Magnitude0
ClinVar
Risk rs796053025(G;G)
Alt rs796053025(G;G)
Reference rs796053025(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166850807T>C
CLNSRC
CLNACC RCV000188971.2,