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rs796053159

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053159(A;A)
Make rs796053159(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165388707
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053159
ebirs796053159
HLIrs796053159
Exacrs796053159
Varsomers796053159
Maprs796053159
PheGenIrs796053159
hapmaprs796053159
1000 genomesrs796053159
hgdprs796053159
ensemblrs796053159
gopubmedrs796053159
geneviewrs796053159
scholarrs796053159
googlers796053159
pharmgkbrs796053159
gwascentralrs796053159
openSNPrs796053159
23andMers796053159
23andMe allrs796053159
SNP Nexus

SNPshotrs796053159
SNPdbers796053159
MSV3drs796053159
GWAS Ctlgrs796053159
Max Magnitude0
ClinVar
Risk rs796053159(A;A)
Alt rs796053159(A;A)
Reference rs796053159(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166245217G>A
CLNSRC
CLNACC RCV000189173.1,