Have questions? Visit https://www.reddit.com/r/SNPedia

rs61889560

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61889560(A;A)
Make rs61889560(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position68423568
GeneLRP5
is asnp
is mentioned by
dbSNPrs61889560
ebirs61889560
HLIrs61889560
Exacrs61889560
Varsomers61889560
Maprs61889560
PheGenIrs61889560
hapmaprs61889560
1000 genomesrs61889560
hgdprs61889560
ensemblrs61889560
gopubmedrs61889560
geneviewrs61889560
scholarrs61889560
googlers61889560
pharmgkbrs61889560
gwascentralrs61889560
openSNPrs61889560
23andMers61889560
23andMe allrs61889560
SNP Nexus

SNPshotrs61889560
SNPdbers61889560
MSV3drs61889560
GWAS Ctlgrs61889560
Max Magnitude0
[PMID 27120077] Exome Sequencing of Familial Bipolar Disorder. The minor allele of this SNP is one of 84 rare variants speculated to have an impact (positive or negative; see publication for specific SNP details) on risk for bipolar disorder. The analysis of many more patients is likely to be required to confirm or refute this association.
ClinVar
Risk rs61889560(A,T;A,T)
Alt rs61889560(A,T;A,T)
Reference rs61889560(G;G)
Significance Untested
Disease Polycystic kidney disease not provided
Variation info
Gene LRP5
CLNDBN Polycystic kidney disease, adult type not provided
Reversed 0
HGVS NC_000011.9:g.68191036G>A
CLNSRC
CLNACC RCV000162089.1, RCV000174732.1,