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rs2214681

From SNPedia

Orientationminus
Stabilizedminus
Make rs2214681(C;C)
Make rs2214681(C;T)
Make rs2214681(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position148005600
GeneCNTNAP2
is asnp
is mentioned by
dbSNPrs2214681
ebirs2214681
HLIrs2214681
Exacrs2214681
Varsomers2214681
Maprs2214681
PheGenIrs2214681
hapmaprs2214681
1000 genomesrs2214681
hgdprs2214681
ensemblrs2214681
gopubmedrs2214681
geneviewrs2214681
scholarrs2214681
googlers2214681
pharmgkbrs2214681
gwascentralrs2214681
openSNPrs2214681
23andMers2214681
23andMe allrs2214681
SNP Nexus

SNPshotrs2214681
SNPdbers2214681
MSV3drs2214681
GWAS Ctlgrs2214681
GMAF0.4426
Max Magnitude
? (C;C) (C;T) (T;T) 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 0.0000030000000000000001
Odds Ratio NR NR


[PMID 21276240OA-icon.png] A validation of the first genome-wide association study of calcaneus ultrasound parameters in the European Male Ageing Study.


GET Evidence
rs2214681
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.484375
summary