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rs181327458

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs181327458(C;T)
Make rs181327458(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position165310448
GeneSCN2A
is asnp
is mentioned by
dbSNPrs181327458
ebirs181327458
HLIrs181327458
Exacrs181327458
Varsomers181327458
Maprs181327458
PheGenIrs181327458
hapmaprs181327458
1000 genomesrs181327458
hgdprs181327458
ensemblrs181327458
gopubmedrs181327458
geneviewrs181327458
scholarrs181327458
googlers181327458
pharmgkbrs181327458
gwascentralrs181327458
openSNPrs181327458
23andMers181327458
23andMe allrs181327458
SNP Nexus

SNPshotrs181327458
SNPdbers181327458
MSV3drs181327458
GWAS Ctlgrs181327458
Max Magnitude0
ClinVar
Risk rs181327458(T;T)
Alt rs181327458(T;T)
Reference rs181327458(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN2A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166166958C>T
CLNSRC
CLNACC RCV000189195.1,