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rs8001611

From SNPedia

Orientationplus
Stabilizedplus
Make rs8001611(C;C)
Make rs8001611(C;T)
Make rs8001611(T;T)
ReferenceGRCh38 38.1/142
Chromosome13
Position42391558
is asnp
is mentioned by
dbSNPrs8001611
ebirs8001611
HLIrs8001611
Exacrs8001611
Varsomers8001611
Maprs8001611
PheGenIrs8001611
hapmaprs8001611
1000 genomesrs8001611
hgdprs8001611
ensemblrs8001611
gopubmedrs8001611
geneviewrs8001611
scholarrs8001611
googlers8001611
pharmgkbrs8001611
gwascentralrs8001611
openSNPrs8001611
23andMers8001611
23andMe allrs8001611
SNP Nexus

SNPshotrs8001611
SNPdbers8001611
MSV3drs8001611
GWAS Ctlgrs8001611
Max Magnitude
GWAS snp
PMID [PMID 23644456]
Trait Bone mineral density
Title Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits.
Risk Allele
P-val 2E-12
Odds Ratio 1.21 [NR]