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rs796053115

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053115(A;A)
Make rs796053115(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165344627
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053115
ebirs796053115
HLIrs796053115
Exacrs796053115
Varsomers796053115
Maprs796053115
PheGenIrs796053115
hapmaprs796053115
1000 genomesrs796053115
hgdprs796053115
ensemblrs796053115
gopubmedrs796053115
geneviewrs796053115
scholarrs796053115
googlers796053115
pharmgkbrs796053115
gwascentralrs796053115
openSNPrs796053115
23andMers796053115
23andMe allrs796053115
SNP Nexus

SNPshotrs796053115
SNPdbers796053115
MSV3drs796053115
GWAS Ctlgrs796053115
Max Magnitude0
ClinVar
Risk rs796053115(A;A)
Alt rs796053115(A;A)
Reference rs796053115(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166201137G>A
CLNSRC
CLNACC RCV000189117.1,