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rs796053179

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053179(C;T)
Make rs796053179(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165313908
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053179
ebirs796053179
HLIrs796053179
Exacrs796053179
Varsomers796053179
Maprs796053179
PheGenIrs796053179
hapmaprs796053179
1000 genomesrs796053179
hgdprs796053179
ensemblrs796053179
gopubmedrs796053179
geneviewrs796053179
scholarrs796053179
googlers796053179
pharmgkbrs796053179
gwascentralrs796053179
openSNPrs796053179
23andMers796053179
23andMe allrs796053179
SNP Nexus

SNPshotrs796053179
SNPdbers796053179
MSV3drs796053179
GWAS Ctlgrs796053179
Max Magnitude0
ClinVar
Risk rs796053179(T;T)
Alt rs796053179(T;T)
Reference rs796053179(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166170418C>T
CLNSRC
CLNACC RCV000189205.1,