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rs796053158

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053158(A;A)
Make rs796053158(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165388701
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053158
ebirs796053158
HLIrs796053158
Exacrs796053158
Varsomers796053158
Maprs796053158
PheGenIrs796053158
hapmaprs796053158
1000 genomesrs796053158
hgdprs796053158
ensemblrs796053158
gopubmedrs796053158
geneviewrs796053158
scholarrs796053158
googlers796053158
pharmgkbrs796053158
gwascentralrs796053158
openSNPrs796053158
23andMers796053158
23andMe allrs796053158
SNP Nexus

SNPshotrs796053158
SNPdbers796053158
MSV3drs796053158
GWAS Ctlgrs796053158
Max Magnitude0
ClinVar
Risk rs796053158(A;A)
Alt rs796053158(A;A)
Reference rs796053158(G;G)
Significance Pathogenic
Disease not specified
Variation info
Gene SCN2A
CLNDBN not specified
Reversed 0
HGVS NC_000002.11:g.166245211G>A
CLNSRC
CLNACC RCV000189172.2,