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rs137854613

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs137854613(C;T)
Make rs137854613(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position38551505
GeneSCN5A
is asnp
is mentioned by
dbSNPrs137854613
ebirs137854613
HLIrs137854613
Exacrs137854613
Varsomers137854613
Maprs137854613
PheGenIrs137854613
hapmaprs137854613
1000 genomesrs137854613
hgdprs137854613
ensemblrs137854613
gopubmedrs137854613
geneviewrs137854613
scholarrs137854613
googlers137854613
pharmgkbrs137854613
gwascentralrs137854613
openSNPrs137854613
23andMers137854613
23andMe allrs137854613
SNP Nexus

SNPshotrs137854613
SNPdbers137854613
MSV3drs137854613
GWAS Ctlgrs137854613
Max Magnitude0
OMIM600163
Desc
Variant0028
Relatedalso
ClinVar
Risk rs137854613(A,T;A,T)
Alt rs137854613(A,T;A,T)
Reference rs137854613(C;C)
Significance Pathogenic
Disease Sick sinus syndrome 1 not provided
Variation info
Gene SCN5A
CLNDBN Sick sinus syndrome 1, autosomal recessive not provided
Reversed 1
HGVS NC_000003.11:g.38592996G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009968.2, RCV000183087.1,