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rs201740080

From SNPedia

Orientationplus
Stabilizedplus
Make rs201740080(C;C)
Make rs201740080(C;T)
Make rs201740080(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position7768947
GeneCLEC4M, LOC105372263
is asnp
is mentioned by
dbSNPrs201740080
dbSNP (old)rs201740080
ClinGenrs201740080
ebirs201740080
HLIrs201740080
Exacrs201740080
Gnomadrs201740080
Varsomers201740080
Maprs201740080
PheGenIrs201740080
Biobankrs201740080
1000 genomesrs201740080
hgdprs201740080
ensemblrs201740080
gopubmedrs201740080
geneviewrs201740080
scholarrs201740080
googlers201740080
pharmgkbrs201740080
gwascentralrs201740080
openSNPrs201740080
23andMers201740080
23andMe allrs201740080
SNP Nexus

SNPshotrs201740080
SNPdbers201740080
MSV3drs201740080
GWAS Ctlgrs201740080
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.