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rs769292594

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs769292594(C;T)
Make rs769292594(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position38603896
GeneSCN5A
is asnp
is mentioned by
dbSNPrs769292594
ebirs769292594
HLIrs769292594
Exacrs769292594
Varsomers769292594
Maprs769292594
PheGenIrs769292594
hapmaprs769292594
1000 genomesrs769292594
hgdprs769292594
ensemblrs769292594
gopubmedrs769292594
geneviewrs769292594
scholarrs769292594
googlers769292594
pharmgkbrs769292594
gwascentralrs769292594
openSNPrs769292594
23andMers769292594
23andMe allrs769292594
SNP Nexus

SNPshotrs769292594
SNPdbers769292594
MSV3drs769292594
GWAS Ctlgrs769292594
Max Magnitude0
ClinVar
Risk rs769292594(T;T)
Alt rs769292594(T;T)
Reference rs769292594(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.38645387C>T
CLNSRC
CLNACC RCV000182983.2,