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rs372395294

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs372395294(C;C)
Make rs372395294(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position38606042
GeneSCN5A
is asnp
is mentioned by
dbSNPrs372395294
ebirs372395294
HLIrs372395294
Exacrs372395294
Varsomers372395294
Maprs372395294
PheGenIrs372395294
hapmaprs372395294
1000 genomesrs372395294
hgdprs372395294
ensemblrs372395294
gopubmedrs372395294
geneviewrs372395294
scholarrs372395294
googlers372395294
pharmgkbrs372395294
gwascentralrs372395294
openSNPrs372395294
23andMers372395294
23andMe allrs372395294
SNP Nexus

SNPshotrs372395294
SNPdbers372395294
MSV3drs372395294
GWAS Ctlgrs372395294
Max Magnitude0
ClinVar
Risk rs372395294(C;C)
Alt rs372395294(C;C)
Reference rs372395294(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.38647533T>C
CLNSRC
CLNACC RCV000182965.2,