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rs796053114

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053114(G;G)
Make rs796053114(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165344596
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053114
ebirs796053114
HLIrs796053114
Exacrs796053114
Varsomers796053114
Maprs796053114
PheGenIrs796053114
hapmaprs796053114
1000 genomesrs796053114
hgdprs796053114
ensemblrs796053114
gopubmedrs796053114
geneviewrs796053114
scholarrs796053114
googlers796053114
pharmgkbrs796053114
gwascentralrs796053114
openSNPrs796053114
23andMers796053114
23andMe allrs796053114
SNP Nexus

SNPshotrs796053114
SNPdbers796053114
MSV3drs796053114
GWAS Ctlgrs796053114
Max Magnitude0
ClinVar
Risk rs796053114(G;G)
Alt rs796053114(G;G)
Reference rs796053114(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166201106T>G
CLNSRC
CLNACC RCV000189116.2,