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rs796053146

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053146(C;T)
Make rs796053146(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165389742
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053146
ebirs796053146
HLIrs796053146
Exacrs796053146
Varsomers796053146
Maprs796053146
PheGenIrs796053146
hapmaprs796053146
1000 genomesrs796053146
hgdprs796053146
ensemblrs796053146
gopubmedrs796053146
geneviewrs796053146
scholarrs796053146
googlers796053146
pharmgkbrs796053146
gwascentralrs796053146
openSNPrs796053146
23andMers796053146
23andMe allrs796053146
SNP Nexus

SNPshotrs796053146
SNPdbers796053146
MSV3drs796053146
GWAS Ctlgrs796053146
Max Magnitude0
ClinVar
Risk rs796053146(T;T)
Alt rs796053146(T;T)
Reference rs796053146(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166246252C>T
CLNSRC
CLNACC RCV000189160.1,