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rs796053117

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053117(A;A)
Make rs796053117(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165344643
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053117
ebirs796053117
HLIrs796053117
Exacrs796053117
Varsomers796053117
Maprs796053117
PheGenIrs796053117
hapmaprs796053117
1000 genomesrs796053117
hgdprs796053117
ensemblrs796053117
gopubmedrs796053117
geneviewrs796053117
scholarrs796053117
googlers796053117
pharmgkbrs796053117
gwascentralrs796053117
openSNPrs796053117
23andMers796053117
23andMe allrs796053117
SNP Nexus

SNPshotrs796053117
SNPdbers796053117
MSV3drs796053117
GWAS Ctlgrs796053117
Max Magnitude0
ClinVar
Risk rs796053117(A;A)
Alt rs796053117(A;A)
Reference rs796053117(T;T)
Significance Probable-Pathogenic
Disease not specified
Variation info
Gene SCN2A
CLNDBN not specified
Reversed 0
HGVS NC_000002.11:g.166201153T>A
CLNSRC
CLNACC RCV000189119.2,