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rs557957405

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs557957405(A;A)
Make rs557957405(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position38576768
GeneSCN5A
is asnp
is mentioned by
dbSNPrs557957405
ebirs557957405
HLIrs557957405
Exacrs557957405
Varsomers557957405
Maprs557957405
PheGenIrs557957405
hapmaprs557957405
1000 genomesrs557957405
hgdprs557957405
ensemblrs557957405
gopubmedrs557957405
geneviewrs557957405
scholarrs557957405
googlers557957405
pharmgkbrs557957405
gwascentralrs557957405
openSNPrs557957405
23andMers557957405
23andMe allrs557957405
SNP Nexus

SNPshotrs557957405
SNPdbers557957405
MSV3drs557957405
GWAS Ctlgrs557957405
Max Magnitude0
ClinVar
Risk rs557957405(A;A)
Alt rs557957405(A;A)
Reference rs557957405(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN5A
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.38618259C>A
CLNSRC
CLNACC RCV000183035.1,