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rs72544145

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs72544145(A;A)
Make rs72544145(A;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position118168739
GeneSCN2B
is asnp
is mentioned by
dbSNPrs72544145
ebirs72544145
HLIrs72544145
Exacrs72544145
Varsomers72544145
Maprs72544145
PheGenIrs72544145
hapmaprs72544145
1000 genomesrs72544145
hgdprs72544145
ensemblrs72544145
gopubmedrs72544145
geneviewrs72544145
scholarrs72544145
googlers72544145
pharmgkbrs72544145
gwascentralrs72544145
openSNPrs72544145
23andMers72544145
23andMe allrs72544145
SNP Nexus

SNPshotrs72544145
SNPdbers72544145
MSV3drs72544145
GWAS Ctlgrs72544145
Max Magnitude0
ClinVar
Risk rs72544145(A;A)
Alt rs72544145(A;A)
Reference rs72544145(G;G)
Significance Pathogenic
Disease Atrial fibrillation
Variation info
Gene SCN2B
CLNDBN Atrial fibrillation, familial, 14
Reversed 1
HGVS NC_000011.9:g.118039454C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000054540.2,