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rs796053181

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053181(C;C)
Make rs796053181(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165313996
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053181
ebirs796053181
HLIrs796053181
Exacrs796053181
Varsomers796053181
Maprs796053181
PheGenIrs796053181
hapmaprs796053181
1000 genomesrs796053181
hgdprs796053181
ensemblrs796053181
gopubmedrs796053181
geneviewrs796053181
scholarrs796053181
googlers796053181
pharmgkbrs796053181
gwascentralrs796053181
openSNPrs796053181
23andMers796053181
23andMe allrs796053181
SNP Nexus

SNPshotrs796053181
SNPdbers796053181
MSV3drs796053181
GWAS Ctlgrs796053181
Max Magnitude0
ClinVar
Risk rs796053181(C;C)
Alt rs796053181(C;C)
Reference rs796053181(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166170506T>C
CLNSRC
CLNACC RCV000189207.2,