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rs796053151

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796053151(A;A)
Make rs796053151(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position165386895
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053151
ebirs796053151
HLIrs796053151
Exacrs796053151
Varsomers796053151
Maprs796053151
PheGenIrs796053151
hapmaprs796053151
1000 genomesrs796053151
hgdprs796053151
ensemblrs796053151
gopubmedrs796053151
geneviewrs796053151
scholarrs796053151
googlers796053151
pharmgkbrs796053151
gwascentralrs796053151
openSNPrs796053151
23andMers796053151
23andMe allrs796053151
SNP Nexus

SNPshotrs796053151
SNPdbers796053151
MSV3drs796053151
GWAS Ctlgrs796053151
Max Magnitude0
ClinVar
Risk rs796053151(A;A)
Alt rs796053151(A;A)
Reference rs796053151(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166243405T>A
CLNSRC
CLNACC RCV000189165.2,