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rs796053186

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053186(C;T)
Make rs796053186(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165315657
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053186
ebirs796053186
HLIrs796053186
Exacrs796053186
Varsomers796053186
Maprs796053186
PheGenIrs796053186
hapmaprs796053186
1000 genomesrs796053186
hgdprs796053186
ensemblrs796053186
gopubmedrs796053186
geneviewrs796053186
scholarrs796053186
googlers796053186
pharmgkbrs796053186
gwascentralrs796053186
openSNPrs796053186
23andMers796053186
23andMe allrs796053186
SNP Nexus

SNPshotrs796053186
SNPdbers796053186
MSV3drs796053186
GWAS Ctlgrs796053186
Max Magnitude0
ClinVar
Risk rs796053186(T;T)
Alt rs796053186(T;T)
Reference rs796053186(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166172167C>T
CLNSRC
CLNACC RCV000189215.1,