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rs150061718

From SNPedia

Orientationplus
Stabilizedplus
Make rs150061718(C;C)
Make rs150061718(C;T)
Make rs150061718(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position98385747
GeneFARP1
is asnp
is mentioned by
dbSNPrs150061718
dbSNP (old)rs150061718
ClinGenrs150061718
ebirs150061718
HLIrs150061718
Exacrs150061718
Gnomadrs150061718
Varsomers150061718
Maprs150061718
PheGenIrs150061718
Biobankrs150061718
1000 genomesrs150061718
hgdprs150061718
ensemblrs150061718
gopubmedrs150061718
geneviewrs150061718
scholarrs150061718
googlers150061718
pharmgkbrs150061718
gwascentralrs150061718
openSNPrs150061718
23andMers150061718
23andMe allrs150061718
SNP Nexus

SNPshotrs150061718
SNPdbers150061718
MSV3drs150061718
GWAS Ctlgrs150061718
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.