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rs796053171

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796053171(G;T)
Make rs796053171(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position165308795
GeneSCN2A
is asnp
is mentioned by
dbSNPrs796053171
ebirs796053171
HLIrs796053171
Exacrs796053171
Varsomers796053171
Maprs796053171
PheGenIrs796053171
hapmaprs796053171
1000 genomesrs796053171
hgdprs796053171
ensemblrs796053171
gopubmedrs796053171
geneviewrs796053171
scholarrs796053171
googlers796053171
pharmgkbrs796053171
gwascentralrs796053171
openSNPrs796053171
23andMers796053171
23andMe allrs796053171
SNP Nexus

SNPshotrs796053171
SNPdbers796053171
MSV3drs796053171
GWAS Ctlgrs796053171
Max Magnitude0
ClinVar
Risk rs796053171(T;T)
Alt rs796053171(T;T)
Reference rs796053171(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166165305G>T
CLNSRC
CLNACC RCV000189192.1,