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rs61757261

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs61757261(G;G)
Make rs61757261(G;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position11847373
GeneNPPA, NPPA-AS1
is asnp
is mentioned by
dbSNPrs61757261
ebirs61757261
HLIrs61757261
Exacrs61757261
Varsomers61757261
Maprs61757261
PheGenIrs61757261
hapmaprs61757261
1000 genomesrs61757261
hgdprs61757261
ensemblrs61757261
gopubmedrs61757261
geneviewrs61757261
scholarrs61757261
googlers61757261
pharmgkbrs61757261
gwascentralrs61757261
openSNPrs61757261
23andMers61757261
23andMe allrs61757261
SNP Nexus

SNPshotrs61757261
SNPdbers61757261
MSV3drs61757261
GWAS Ctlgrs61757261
Max Magnitude0
ClinVar
Risk rs61757261(G;G)
Alt rs61757261(G;G)
Reference rs61757261(T;T)
Significance Other
Disease Atrial fibrillation
Variation info
Gene NPPA NPPA-AS1
CLNDBN Atrial fibrillation, familial, 6
Reversed 0
HGVS NC_000001.10:g.11907430T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000114741.3,