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rs796053203

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053203(G;G)
Make rs796053203(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165309393
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053203
ebirs796053203
HLIrs796053203
Exacrs796053203
Varsomers796053203
Maprs796053203
PheGenIrs796053203
hapmaprs796053203
1000 genomesrs796053203
hgdprs796053203
ensemblrs796053203
gopubmedrs796053203
geneviewrs796053203
scholarrs796053203
googlers796053203
pharmgkbrs796053203
gwascentralrs796053203
openSNPrs796053203
23andMers796053203
23andMe allrs796053203
SNP Nexus

SNPshotrs796053203
SNPdbers796053203
MSV3drs796053203
GWAS Ctlgrs796053203
Max Magnitude0
ClinVar
Risk rs796053203(G;G)
Alt rs796053203(G;G)
Reference rs796053203(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166165903T>G
CLNSRC
CLNACC RCV000189243.2,