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rs796053160

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796053160(C;G)
Make rs796053160(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165388714
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053160
ebirs796053160
HLIrs796053160
Exacrs796053160
Varsomers796053160
Maprs796053160
PheGenIrs796053160
hapmaprs796053160
1000 genomesrs796053160
hgdprs796053160
ensemblrs796053160
gopubmedrs796053160
geneviewrs796053160
scholarrs796053160
googlers796053160
pharmgkbrs796053160
gwascentralrs796053160
openSNPrs796053160
23andMers796053160
23andMe allrs796053160
SNP Nexus

SNPshotrs796053160
SNPdbers796053160
MSV3drs796053160
GWAS Ctlgrs796053160
Max Magnitude0
ClinVar
Risk rs796053160(G;G)
Alt rs796053160(G;G)
Reference rs796053160(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166245224C>G
CLNSRC
CLNACC RCV000189174.2,