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rs2037892

From SNPedia

Orientationminus
Stabilizedminus
Make rs2037892(C;C)
Make rs2037892(C;T)
Make rs2037892(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position122370213
is asnp
is mentioned by
dbSNPrs2037892
ebirs2037892
HLIrs2037892
Exacrs2037892
Varsomers2037892
Maprs2037892
PheGenIrs2037892
hapmaprs2037892
1000 genomesrs2037892
hgdprs2037892
ensemblrs2037892
gopubmedrs2037892
geneviewrs2037892
scholarrs2037892
googlers2037892
pharmgkbrs2037892
gwascentralrs2037892
openSNPrs2037892
23andMers2037892
23andMe allrs2037892
SNP Nexus

SNPshotrs2037892
SNPdbers2037892
MSV3drs2037892
GWAS Ctlgrs2037892
GMAF0.2695
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22903471OA-icon.png]
Trait Lentiform nucleus volume
Title Genome-wide association identifies genetic variants associated with lentiform nucleus volume in N = 1345 young and elderly subjects.
Risk Allele A
P-val 5E-6
Odds Ratio 156.70 [NR] unit increase