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rs377325221

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs377325221(A;A)
Make rs377325221(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position165994205
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs377325221
ebirs377325221
HLIrs377325221
Exacrs377325221
Varsomers377325221
Maprs377325221
PheGenIrs377325221
hapmaprs377325221
1000 genomesrs377325221
hgdprs377325221
ensemblrs377325221
gopubmedrs377325221
geneviewrs377325221
scholarrs377325221
googlers377325221
pharmgkbrs377325221
gwascentralrs377325221
openSNPrs377325221
23andMers377325221
23andMe allrs377325221
SNP Nexus

SNPshotrs377325221
SNPdbers377325221
MSV3drs377325221
GWAS Ctlgrs377325221
Max Magnitude0
ClinVar
Risk rs377325221(A;A)
Alt rs377325221(A;A)
Reference rs377325221(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.166850715T>A
CLNSRC
CLNACC RCV000188979.2,