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rs7895307

From SNPedia

Orientationplus
Make rs7895307(A;A)
Make rs7895307(A;G)
Make rs7895307(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position112984202
GeneTCF7L2
is asnp
is mentioned by
dbSNPrs7895307
ebirs7895307
HLIrs7895307
Exacrs7895307
Varsomers7895307
Maprs7895307
PheGenIrs7895307
hapmaprs7895307
1000 genomesrs7895307
hgdprs7895307
ensemblrs7895307
gopubmedrs7895307
geneviewrs7895307
scholarrs7895307
googlers7895307
pharmgkbrs7895307
gwascentralrs7895307
openSNPrs7895307
23andMers7895307
23andMe allrs7895307
SNP Nexus

SNPshotrs7895307
SNPdbers7895307
MSV3drs7895307
GWAS Ctlgrs7895307
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 26934194] Accumulating evidence for a role of TCF7L2 variants in bipolar disorder with elevated body mass index.