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rs796053135

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796053135(A;G)
Make rs796053135(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165374748
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053135
ebirs796053135
HLIrs796053135
Exacrs796053135
Varsomers796053135
Maprs796053135
PheGenIrs796053135
hapmaprs796053135
1000 genomesrs796053135
hgdprs796053135
ensemblrs796053135
gopubmedrs796053135
geneviewrs796053135
scholarrs796053135
googlers796053135
pharmgkbrs796053135
gwascentralrs796053135
openSNPrs796053135
23andMers796053135
23andMe allrs796053135
SNP Nexus

SNPshotrs796053135
SNPdbers796053135
MSV3drs796053135
GWAS Ctlgrs796053135
Max Magnitude0
ClinVar
Risk rs796053135(G;G)
Alt rs796053135(G;G)
Reference rs796053135(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166231258A>G
CLNSRC
CLNACC RCV000189148.2,