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rs796053182

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796053182(A;G)
Make rs796053182(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165314008
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053182
ebirs796053182
HLIrs796053182
Exacrs796053182
Varsomers796053182
Maprs796053182
PheGenIrs796053182
hapmaprs796053182
1000 genomesrs796053182
hgdprs796053182
ensemblrs796053182
gopubmedrs796053182
geneviewrs796053182
scholarrs796053182
googlers796053182
pharmgkbrs796053182
gwascentralrs796053182
openSNPrs796053182
23andMers796053182
23andMe allrs796053182
SNP Nexus

SNPshotrs796053182
SNPdbers796053182
MSV3drs796053182
GWAS Ctlgrs796053182
Max Magnitude0
ClinVar
Risk rs796053182(G;G)
Alt rs796053182(G;G)
Reference rs796053182(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166170518A>G
CLNSRC
CLNACC RCV000189208.1,