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rs587776851

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(AAG;AAG) 0 common in clinvar
(TT;TT) 0 common in clinvar
Make rs587776851(-;-)
Make rs587776851(-;TT)
ReferenceGRCh38 38.1/142
Chromosome1
Position11846008
GeneNPPA-AS1
is asnp
is mentioned by
dbSNPrs587776851
ebirs587776851
HLIrs587776851
Exacrs587776851
Varsomers587776851
Maprs587776851
PheGenIrs587776851
hapmaprs587776851
1000 genomesrs587776851
hgdprs587776851
ensemblrs587776851
gopubmedrs587776851
geneviewrs587776851
scholarrs587776851
googlers587776851
pharmgkbrs587776851
gwascentralrs587776851
openSNPrs587776851
23andMers587776851
23andMe allrs587776851
SNP Nexus

SNPshotrs587776851
SNPdbers587776851
MSV3drs587776851
GWAS Ctlgrs587776851
Max Magnitude0
ClinVar
Risk rs587776851(TTG,G;TTG,G)
Alt rs587776851(TTG,G;TTG,G)
Reference rs587776851(AAG;AAG)
Significance Pathogenic
Disease Atrial fibrillation
Variation info
Gene NPPA-AS1
CLNDBN Atrial fibrillation, familial, 6
Reversed 1
HGVS NC_000001.10:g.11906065_11906066delTT
CLNSRC OMIM Allelic Variant
CLNACC RCV000019366.23,