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rs1386498

From SNPedia

Orientationplus
Stabilizedplus
Make rs1386498(A;A)
Make rs1386498(A;G)
Make rs1386498(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position72004363
GeneTPH2
is asnp
is mentioned by
dbSNPrs1386498
ebirs1386498
HLIrs1386498
Exacrs1386498
Varsomers1386498
Maprs1386498
PheGenIrs1386498
hapmaprs1386498
1000 genomesrs1386498
hgdprs1386498
ensemblrs1386498
gopubmedrs1386498
geneviewrs1386498
scholarrs1386498
googlers1386498
pharmgkbrs1386498
gwascentralrs1386498
openSNPrs1386498
23andMers1386498
23andMe allrs1386498
SNP Nexus

SNPshotrs1386498
SNPdbers1386498
MSV3drs1386498
GWAS Ctlgrs1386498
GMAF0.4986
Max Magnitude
? (A;A) (A;G) (G;G) 28

[PMID 21396719] Influence of TPH2 variants on diagnosis and response to treatment in patients with major depression, bipolar disorder and schizophrenia