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rs796053112

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796053112(A;G)
Make rs796053112(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165342387
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053112
ebirs796053112
HLIrs796053112
Exacrs796053112
Varsomers796053112
Maprs796053112
PheGenIrs796053112
hapmaprs796053112
1000 genomesrs796053112
hgdprs796053112
ensemblrs796053112
gopubmedrs796053112
geneviewrs796053112
scholarrs796053112
googlers796053112
pharmgkbrs796053112
gwascentralrs796053112
openSNPrs796053112
23andMers796053112
23andMe allrs796053112
SNP Nexus

SNPshotrs796053112
SNPdbers796053112
MSV3drs796053112
GWAS Ctlgrs796053112
Max Magnitude0
ClinVar
Risk rs796053112(G;G)
Alt rs796053112(G;G)
Reference rs796053112(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166198897A>G
CLNSRC
CLNACC RCV000189114.1,