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rs9426935

From SNPedia

Orientationplus
Stabilizedplus
Make rs9426935(C;C)
Make rs9426935(C;T)
Make rs9426935(T;T)
ReferenceGRCh37.p5 37.3/137
Chromosome1
Position153796924
GeneLOC105371448
is asnp
is mentioned by
dbSNPrs9426935
dbSNP (classic)rs9426935
ClinGenrs9426935
ebirs9426935
HLIrs9426935
Exacrs9426935
Gnomadrs9426935
Varsomers9426935
LitVarrs9426935
Maprs9426935
PheGenIrs9426935
Biobankrs9426935
1000 genomesrs9426935
hgdprs9426935
ensemblrs9426935
geneviewrs9426935
scholarrs9426935
googlers9426935
pharmgkbrs9426935
gwascentralrs9426935
openSNPrs9426935
23andMers9426935
SNPshotrs9426935
SNPdbers9426935
MSV3drs9426935
GWAS Ctlgrs9426935
GMAF0.3072
Max Magnitude0
? (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 C
P-val 5E-6
Odds Ratio 96.63 [NR] unit decrease


[PMID 18505370OA-icon.png] Identification of a linkage disequilibrium block in chromosome 1q associated with BMD in premenopausal white women.