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rs6735786

From SNPedia

Orientationplus
Stabilizedplus
Make rs6735786(C;C)
Make rs6735786(C;T)
Make rs6735786(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position103153780
is asnp
is mentioned by
dbSNPrs6735786
ebirs6735786
HLIrs6735786
Exacrs6735786
Varsomers6735786
Maprs6735786
PheGenIrs6735786
hapmaprs6735786
1000 genomesrs6735786
hgdprs6735786
ensemblrs6735786
gopubmedrs6735786
geneviewrs6735786
scholarrs6735786
googlers6735786
pharmgkbrs6735786
gwascentralrs6735786
openSNPrs6735786
23andMers6735786
23andMe allrs6735786
SNP Nexus

SNPshotrs6735786
SNPdbers6735786
MSV3drs6735786
GWAS Ctlgrs6735786
GMAF0.4036
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 19079262]
Trait Bone mineral density (hip)
Title New sequence variants associated with bone mineral density
Risk Allele C
P-val 0.000002
Odds Ratio 0.07 [0.04-0.09] SD decrease



GET Evidence
rs6735786
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.278689
summary