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rs922948

From SNPedia

Orientationminus
Stabilizedminus
Make rs922948(C;C)
Make rs922948(C;T)
Make rs922948(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position69393486
GeneFRMD4B
is asnp
is mentioned by
dbSNPrs922948
ebirs922948
HLIrs922948
Exacrs922948
Varsomers922948
Maprs922948
PheGenIrs922948
hapmaprs922948
1000 genomesrs922948
hgdprs922948
ensemblrs922948
gopubmedrs922948
geneviewrs922948
scholarrs922948
googlers922948
pharmgkbrs922948
gwascentralrs922948
openSNPrs922948
23andMers922948
23andMe allrs922948
SNP Nexus

SNPshotrs922948
SNPdbers922948
MSV3drs922948
GWAS Ctlgrs922948
GMAF0.3044
Max Magnitude
? (C;C) (C;T) (T;T) 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 0.0000019999999999999999
Odds Ratio NR NR


GET Evidence
rs922948
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.734375
summary