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rs141679163

From SNPedia

Orientationplus
Stabilizedplus
Make rs141679163(G;G)
Make rs141679163(G;T)
Make rs141679163(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position183240079
GeneLAMC2
is asnp
is mentioned by
dbSNPrs141679163
dbSNP (old)rs141679163
ClinGenrs141679163
ebirs141679163
HLIrs141679163
Exacrs141679163
Varsomers141679163
Maprs141679163
PheGenIrs141679163
Biobankrs141679163
1000 genomesrs141679163
hgdprs141679163
ensemblrs141679163
gopubmedrs141679163
geneviewrs141679163
scholarrs141679163
googlers141679163
pharmgkbrs141679163
gwascentralrs141679163
openSNPrs141679163
23andMers141679163
23andMe allrs141679163
SNP Nexus

SNPshotrs141679163
SNPdbers141679163
MSV3drs141679163
GWAS Ctlgrs141679163
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.