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rs796053140

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796053140(A;G)
Make rs796053140(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165380738
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053140
ebirs796053140
HLIrs796053140
Exacrs796053140
Varsomers796053140
Maprs796053140
PheGenIrs796053140
hapmaprs796053140
1000 genomesrs796053140
hgdprs796053140
ensemblrs796053140
gopubmedrs796053140
geneviewrs796053140
scholarrs796053140
googlers796053140
pharmgkbrs796053140
gwascentralrs796053140
openSNPrs796053140
23andMers796053140
23andMe allrs796053140
SNP Nexus

SNPshotrs796053140
SNPdbers796053140
MSV3drs796053140
GWAS Ctlgrs796053140
Max Magnitude0
ClinVar
Risk rs796053140(G;G)
Alt rs796053140(G;G)
Reference rs796053140(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166237248A>G
CLNSRC
CLNACC RCV000189153.2,