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rs796053155

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053155(A;A)
Make rs796053155(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165388683
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053155
ebirs796053155
HLIrs796053155
Exacrs796053155
Varsomers796053155
Maprs796053155
PheGenIrs796053155
hapmaprs796053155
1000 genomesrs796053155
hgdprs796053155
ensemblrs796053155
gopubmedrs796053155
geneviewrs796053155
scholarrs796053155
googlers796053155
pharmgkbrs796053155
gwascentralrs796053155
openSNPrs796053155
23andMers796053155
23andMe allrs796053155
SNP Nexus

SNPshotrs796053155
SNPdbers796053155
MSV3drs796053155
GWAS Ctlgrs796053155
Max Magnitude0
ClinVar
Risk rs796053155(A;A)
Alt rs796053155(A;A)
Reference rs796053155(G;G)
Significance Other
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166245193G>A
CLNSRC
CLNACC RCV000189169.1,