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

rs796052990

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052990(C;T)
Make rs796052990(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position166036511
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs796052990
ebirs796052990
HLIrs796052990
Exacrs796052990
Varsomers796052990
Maprs796052990
PheGenIrs796052990
hapmaprs796052990
1000 genomesrs796052990
hgdprs796052990
ensemblrs796052990
gopubmedrs796052990
geneviewrs796052990
scholarrs796052990
googlers796052990
pharmgkbrs796052990
gwascentralrs796052990
openSNPrs796052990
23andMers796052990
23andMe allrs796052990
SNP Nexus

SNPshotrs796052990
SNPdbers796052990
MSV3drs796052990
GWAS Ctlgrs796052990
Max Magnitude0
ClinVar
Risk rs796052990(T;T)
Alt rs796052990(T;T)
Reference rs796052990(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166893021G>A
CLNSRC
CLNACC RCV000188905.2,