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rs796053134

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053134(C;C)
Make rs796053134(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165374737
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053134
ebirs796053134
HLIrs796053134
Exacrs796053134
Varsomers796053134
Maprs796053134
PheGenIrs796053134
hapmaprs796053134
1000 genomesrs796053134
hgdprs796053134
ensemblrs796053134
gopubmedrs796053134
geneviewrs796053134
scholarrs796053134
googlers796053134
pharmgkbrs796053134
gwascentralrs796053134
openSNPrs796053134
23andMers796053134
23andMe allrs796053134
SNP Nexus

SNPshotrs796053134
SNPdbers796053134
MSV3drs796053134
GWAS Ctlgrs796053134
Max Magnitude0
ClinVar
Risk rs796053134(C;C)
Alt rs796053134(C;C)
Reference rs796053134(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166231247T>C
CLNSRC
CLNACC RCV000189147.1,