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rs796053153

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053153(C;T)
Make rs796053153(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165386945
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053153
ebirs796053153
HLIrs796053153
Exacrs796053153
Varsomers796053153
Maprs796053153
PheGenIrs796053153
hapmaprs796053153
1000 genomesrs796053153
hgdprs796053153
ensemblrs796053153
gopubmedrs796053153
geneviewrs796053153
scholarrs796053153
googlers796053153
pharmgkbrs796053153
gwascentralrs796053153
openSNPrs796053153
23andMers796053153
23andMe allrs796053153
SNP Nexus

SNPshotrs796053153
SNPdbers796053153
MSV3drs796053153
GWAS Ctlgrs796053153
Max Magnitude0
ClinVar
Risk rs796053153(T;T)
Alt rs796053153(T;T)
Reference rs796053153(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166243455C>T
CLNSRC
CLNACC RCV000189167.1,