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rs796053143

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053143(G;G)
Make rs796053143(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165380677
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053143
ebirs796053143
HLIrs796053143
Exacrs796053143
Varsomers796053143
Maprs796053143
PheGenIrs796053143
hapmaprs796053143
1000 genomesrs796053143
hgdprs796053143
ensemblrs796053143
gopubmedrs796053143
geneviewrs796053143
scholarrs796053143
googlers796053143
pharmgkbrs796053143
gwascentralrs796053143
openSNPrs796053143
23andMers796053143
23andMe allrs796053143
SNP Nexus

SNPshotrs796053143
SNPdbers796053143
MSV3drs796053143
GWAS Ctlgrs796053143
Max Magnitude0
ClinVar
Risk rs796053143(G;G)
Alt rs796053143(G;G)
Reference rs796053143(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166237187T>G
CLNSRC
CLNACC RCV000189156.2,