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

rs796053144

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053144(A;A)
Make rs796053144(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165381109
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053144
ebirs796053144
HLIrs796053144
Exacrs796053144
Varsomers796053144
Maprs796053144
PheGenIrs796053144
hapmaprs796053144
1000 genomesrs796053144
hgdprs796053144
ensemblrs796053144
gopubmedrs796053144
geneviewrs796053144
scholarrs796053144
googlers796053144
pharmgkbrs796053144
gwascentralrs796053144
openSNPrs796053144
23andMers796053144
23andMe allrs796053144
SNP Nexus

SNPshotrs796053144
SNPdbers796053144
MSV3drs796053144
GWAS Ctlgrs796053144
Max Magnitude0
ClinVar
Risk rs796053144(A;A)
Alt rs796053144(A;A)
Reference rs796053144(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166237619T>A
CLNSRC
CLNACC RCV000189157.1,