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rs140002868

From SNPedia

Orientationplus
Stabilizedplus
Make rs140002868(A;A)
Make rs140002868(A;G)
Make rs140002868(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome12
Position131840590
GeneMMP17
is asnp
is mentioned by
dbSNPrs140002868
dbSNP (old)rs140002868
ClinGenrs140002868
ebirs140002868
HLIrs140002868
Exacrs140002868
Gnomadrs140002868
Varsomers140002868
Maprs140002868
PheGenIrs140002868
Biobankrs140002868
1000 genomesrs140002868
hgdprs140002868
ensemblrs140002868
gopubmedrs140002868
geneviewrs140002868
scholarrs140002868
googlers140002868
pharmgkbrs140002868
gwascentralrs140002868
openSNPrs140002868
23andMers140002868
23andMe allrs140002868
SNP Nexus

SNPshotrs140002868
SNPdbers140002868
MSV3drs140002868
GWAS Ctlgrs140002868
Max Magnitude
[PMID 27120077OA-icon.png] Exome Sequencing of Familial Bipolar Disorder. The minor allele of this SNP is one of 84 rare variants speculated to have an impact (positive or negative; see publication for specific SNP details) on risk for bipolar disorder. The analysis of many more patients is likely to be required to confirm or refute this association.