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rs587777339

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587777339(C;T)
Make rs587777339(T;T)
ReferenceGRCh38 38.1/142
Chromosome5
Position37341164
GeneNUP155
is asnp
is mentioned by
dbSNPrs587777339
ebirs587777339
HLIrs587777339
Exacrs587777339
Varsomers587777339
Maprs587777339
PheGenIrs587777339
hapmaprs587777339
1000 genomesrs587777339
hgdprs587777339
ensemblrs587777339
gopubmedrs587777339
geneviewrs587777339
scholarrs587777339
googlers587777339
pharmgkbrs587777339
gwascentralrs587777339
openSNPrs587777339
23andMers587777339
23andMe allrs587777339
SNP Nexus

SNPshotrs587777339
SNPdbers587777339
MSV3drs587777339
GWAS Ctlgrs587777339
Max Magnitude0
ClinVar
Risk rs587777339(C,T;C,T)
Alt rs587777339(C,T;C,T)
Reference rs587777339(G;G)
Significance Pathogenic
Disease Atrial fibrillation
Variation info
Gene NUP155
CLNDBN Atrial fibrillation, familial, 15
Reversed 1
HGVS NC_000005.9:g.37341266C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000114997.3,