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rs796053149

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796053149(A;G)
Make rs796053149(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165386824
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053149
ebirs796053149
HLIrs796053149
Exacrs796053149
Varsomers796053149
Maprs796053149
PheGenIrs796053149
hapmaprs796053149
1000 genomesrs796053149
hgdprs796053149
ensemblrs796053149
gopubmedrs796053149
geneviewrs796053149
scholarrs796053149
googlers796053149
pharmgkbrs796053149
gwascentralrs796053149
openSNPrs796053149
23andMers796053149
23andMe allrs796053149
SNP Nexus

SNPshotrs796053149
SNPdbers796053149
MSV3drs796053149
GWAS Ctlgrs796053149
Max Magnitude0
ClinVar
Risk rs796053149(G;G)
Alt rs796053149(G;G)
Reference rs796053149(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166243334A>G
CLNSRC
CLNACC RCV000189163.2,