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rs796053119

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053119(C;C)
Make rs796053119(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165344707
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053119
ebirs796053119
HLIrs796053119
Exacrs796053119
Varsomers796053119
Maprs796053119
PheGenIrs796053119
hapmaprs796053119
1000 genomesrs796053119
hgdprs796053119
ensemblrs796053119
gopubmedrs796053119
geneviewrs796053119
scholarrs796053119
googlers796053119
pharmgkbrs796053119
gwascentralrs796053119
openSNPrs796053119
23andMers796053119
23andMe allrs796053119
SNP Nexus

SNPshotrs796053119
SNPdbers796053119
MSV3drs796053119
GWAS Ctlgrs796053119
Max Magnitude0
ClinVar
Risk rs796053119(C;C)
Alt rs796053119(C;C)
Reference rs796053119(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166201217G>C
CLNSRC
CLNACC RCV000189122.1,