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rs6600671

From SNPedia

Orientationminus
Stabilizedminus
Make rs6600671(A;A)
Make rs6600671(A;C)
Make rs6600671(C;C)
ReferenceGRCh38 38.1/141
Chromosome1
Position121458637
is asnp
is mentioned by
dbSNPrs6600671
ebirs6600671
HLIrs6600671
Exacrs6600671
Varsomers6600671
Maprs6600671
PheGenIrs6600671
hapmaprs6600671
1000 genomesrs6600671
hgdprs6600671
ensemblrs6600671
gopubmedrs6600671
geneviewrs6600671
scholarrs6600671
googlers6600671
pharmgkbrs6600671
gwascentralrs6600671
openSNPrs6600671
23andMers6600671
23andMe allrs6600671
SNP Nexus

SNPshotrs6600671
SNPdbers6600671
MSV3drs6600671
GWAS Ctlgrs6600671
GMAF0.3131
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 17903296OA-icon.png]
Trait Hip geometry
Title Genome-wide association with bone mass and geometry in the Framingham Heart Study
Risk Allele
P-val 5.9999999999999997E-7
Odds Ratio NR NR


GET Evidence
rs6600671
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.375
summary