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rs796053152

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053152(C;C)
Make rs796053152(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165386912
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053152
ebirs796053152
HLIrs796053152
Exacrs796053152
Varsomers796053152
Maprs796053152
PheGenIrs796053152
hapmaprs796053152
1000 genomesrs796053152
hgdprs796053152
ensemblrs796053152
gopubmedrs796053152
geneviewrs796053152
scholarrs796053152
googlers796053152
pharmgkbrs796053152
gwascentralrs796053152
openSNPrs796053152
23andMers796053152
23andMe allrs796053152
SNP Nexus

SNPshotrs796053152
SNPdbers796053152
MSV3drs796053152
GWAS Ctlgrs796053152
Max Magnitude0
ClinVar
Risk rs796053152(C;C)
Alt rs796053152(C;C)
Reference rs796053152(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166243422T>C
CLNSRC
CLNACC RCV000189166.2,