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rs537423012

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs537423012(C;T)
Make rs537423012(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position38562452
GeneSCN5A
is asnp
is mentioned by
dbSNPrs537423012
ebirs537423012
HLIrs537423012
Exacrs537423012
Varsomers537423012
Maprs537423012
PheGenIrs537423012
hapmaprs537423012
1000 genomesrs537423012
hgdprs537423012
ensemblrs537423012
gopubmedrs537423012
geneviewrs537423012
scholarrs537423012
googlers537423012
pharmgkbrs537423012
gwascentralrs537423012
openSNPrs537423012
23andMers537423012
23andMe allrs537423012
SNP Nexus

SNPshotrs537423012
SNPdbers537423012
MSV3drs537423012
GWAS Ctlgrs537423012
Max Magnitude0
ClinVar
Risk rs537423012(T;T)
Alt rs537423012(T;T)
Reference rs537423012(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.38603943C>T
CLNSRC
CLNACC RCV000183051.2,