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rs796053120

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053120(A;A)
Make rs796053120(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165344687
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053120
ebirs796053120
HLIrs796053120
Exacrs796053120
Varsomers796053120
Maprs796053120
PheGenIrs796053120
hapmaprs796053120
1000 genomesrs796053120
hgdprs796053120
ensemblrs796053120
gopubmedrs796053120
geneviewrs796053120
scholarrs796053120
googlers796053120
pharmgkbrs796053120
gwascentralrs796053120
openSNPrs796053120
23andMers796053120
23andMe allrs796053120
SNP Nexus

SNPshotrs796053120
SNPdbers796053120
MSV3drs796053120
GWAS Ctlgrs796053120
Max Magnitude0
ClinVar
Risk rs796053120(A;A)
Alt rs796053120(A;A)
Reference rs796053120(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166201197G>A
CLNSRC
CLNACC RCV000189123.1,