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rs751787337

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs751787337(C;T)
Make rs751787337(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position38555686
GeneSCN5A
is asnp
is mentioned by
dbSNPrs751787337
ebirs751787337
HLIrs751787337
Exacrs751787337
Varsomers751787337
Maprs751787337
PheGenIrs751787337
hapmaprs751787337
1000 genomesrs751787337
hgdprs751787337
ensemblrs751787337
gopubmedrs751787337
geneviewrs751787337
scholarrs751787337
googlers751787337
pharmgkbrs751787337
gwascentralrs751787337
openSNPrs751787337
23andMers751787337
23andMe allrs751787337
SNP Nexus

SNPshotrs751787337
SNPdbers751787337
MSV3drs751787337
GWAS Ctlgrs751787337
Max Magnitude0
ClinVar
Risk rs751787337(A,T;A,T)
Alt rs751787337(A,T;A,T)
Reference rs751787337(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.38597177C>A
CLNSRC
CLNACC RCV000183080.1,