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rs150546245

From SNPedia

Orientationplus
Stabilizedplus
Make rs150546245(C;C)
Make rs150546245(C;T)
Make rs150546245(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position112148193
GeneLAMA4, LOC107986633
is asnp
is mentioned by
dbSNPrs150546245
dbSNP (old)rs150546245
ClinGenrs150546245
ebirs150546245
HLIrs150546245
Exacrs150546245
Varsomers150546245
Maprs150546245
PheGenIrs150546245
Biobankrs150546245
1000 genomesrs150546245
hgdprs150546245
ensemblrs150546245
gopubmedrs150546245
geneviewrs150546245
scholarrs150546245
googlers150546245
pharmgkbrs150546245
gwascentralrs150546245
openSNPrs150546245
23andMers150546245
23andMe allrs150546245
SNP Nexus

SNPshotrs150546245
SNPdbers150546245
MSV3drs150546245
GWAS Ctlgrs150546245
Max Magnitude
[PMID 27120077] 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.