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rs369365976

From SNPedia

Orientationplus
Stabilizedplus
Make rs369365976(A;A)
Make rs369365976(A;G)
Make rs369365976(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position112472842
GeneIFRD1
is asnp
is mentioned by
dbSNPrs369365976
dbSNP (old)rs369365976
ClinGenrs369365976
ebirs369365976
HLIrs369365976
Exacrs369365976
Gnomadrs369365976
Varsomers369365976
Maprs369365976
PheGenIrs369365976
Biobankrs369365976
1000 genomesrs369365976
hgdprs369365976
ensemblrs369365976
gopubmedrs369365976
geneviewrs369365976
scholarrs369365976
googlers369365976
pharmgkbrs369365976
gwascentralrs369365976
openSNPrs369365976
23andMers369365976
23andMe allrs369365976
SNP Nexus

SNPshotrs369365976
SNPdbers369365976
MSV3drs369365976
GWAS Ctlgrs369365976
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.