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rs10506701

From SNPedia

Orientationminus
Stabilizedminus
Make rs10506701(A;A)
Make rs10506701(A;C)
Make rs10506701(C;C)
ReferenceGRCh38 38.1/141
Chromosome12
Position74192430
GeneFTH1P24
is asnp
is mentioned by
dbSNPrs10506701
ebirs10506701
HLIrs10506701
Exacrs10506701
Varsomers10506701
Maprs10506701
PheGenIrs10506701
hapmaprs10506701
1000 genomesrs10506701
hgdprs10506701
ensemblrs10506701
gopubmedrs10506701
geneviewrs10506701
scholarrs10506701
googlers10506701
pharmgkbrs10506701
gwascentralrs10506701
openSNPrs10506701
23andMers10506701
23andMe allrs10506701
SNP Nexus

SNPshotrs10506701
SNPdbers10506701
MSV3drs10506701
GWAS Ctlgrs10506701
GMAF0.1134
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 17903296OA-icon.png]
Trait Bone mineral density
Title Genome-wide association with bone mass and geometry in the Framingham Heart Study
Risk Allele
P-val 9.9999999999999995E-7
Odds Ratio NR NR


[PMID 19629617OA-icon.png] Replication study of candidate genes/loci associated with osteoporosis based on genome-wide screening.


GET Evidence
rs10506701
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.126984
summary