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rs6710518

From SNPedia

Orientationplus
Stabilizedplus
Make rs6710518(C;C)
Make rs6710518(C;T)
Make rs6710518(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position165726734
is asnp
is mentioned by
dbSNPrs6710518
dbSNP (classic)rs6710518
ClinGenrs6710518
ebirs6710518
HLIrs6710518
Exacrs6710518
Gnomadrs6710518
Varsomers6710518
LitVarrs6710518
Maprs6710518
PheGenIrs6710518
Biobankrs6710518
1000 genomesrs6710518
hgdprs6710518
ensemblrs6710518
geneviewrs6710518
scholarrs6710518
googlers6710518
pharmgkbrs6710518
gwascentralrs6710518
openSNPrs6710518
23andMers6710518
SNPshotrs6710518
SNPdbers6710518
MSV3drs6710518
GWAS Ctlgrs6710518
GMAF0.3604
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 21533022OA-icon.png]
Trait
Title Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk.
Risk Allele T
P-val 5E-10
Odds Ratio 0.0640 [NR] unit decrease