Have questions? Visit https://www.reddit.com/r/SNPedia

rs764659822

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs764659822(A;A)
Make rs764659822(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position103658260
GeneTACR3
is asnp
is mentioned by
dbSNPrs764659822
ebirs764659822
HLIrs764659822
Exacrs764659822
Varsomers764659822
Maprs764659822
PheGenIrs764659822
hapmaprs764659822
1000 genomesrs764659822
hgdprs764659822
ensemblrs764659822
gopubmedrs764659822
geneviewrs764659822
scholarrs764659822
googlers764659822
pharmgkbrs764659822
gwascentralrs764659822
openSNPrs764659822
23andMers764659822
23andMe allrs764659822
SNP Nexus

SNPshotrs764659822
SNPdbers764659822
MSV3drs764659822
GWAS Ctlgrs764659822
Max Magnitude0
ClinVar
Risk rs764659822(A;A)
Alt rs764659822(A;A)
Reference rs764659822(G;G)
Significance Probable-Pathogenic
Disease Hypogonadotropic hypogonadism 11 with or without anosmia
Variation info
Gene TACR3
CLNDBN Hypogonadotropic hypogonadism 11 with or without anosmia
Reversed 0
HGVS NC_000004.11:g.104579417G>A
CLNSRC
CLNACC RCV000200961.1,