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

rs796052997

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052997(G;G)
Make rs796052997(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166013766
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796052997
ebirs796052997
HLIrs796052997
Exacrs796052997
Varsomers796052997
Maprs796052997
PheGenIrs796052997
hapmaprs796052997
1000 genomesrs796052997
hgdprs796052997
ensemblrs796052997
gopubmedrs796052997
geneviewrs796052997
scholarrs796052997
googlers796052997
pharmgkbrs796052997
gwascentralrs796052997
openSNPrs796052997
23andMers796052997
23andMe allrs796052997
SNP Nexus

SNPshotrs796052997
SNPdbers796052997
MSV3drs796052997
GWAS Ctlgrs796052997
Max Magnitude0
ClinVar
Risk rs796052997(G;G)
Alt rs796052997(G;G)
Reference rs796052997(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166870276A>C
CLNSRC
CLNACC RCV000188923.2,