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

rs7702192

From SNPedia

Orientationplus
Stabilizedplus
Make rs7702192(A;A)
Make rs7702192(A;C)
Make rs7702192(C;C)
ReferenceGRCh38 38.1/141
Chromosome5
Position77258982
GenePDE8B
is asnp
is mentioned by
dbSNPrs7702192
ebirs7702192
HLIrs7702192
Exacrs7702192
Varsomers7702192
Maprs7702192
PheGenIrs7702192
hapmaprs7702192
1000 genomesrs7702192
hgdprs7702192
ensemblrs7702192
gopubmedrs7702192
geneviewrs7702192
scholarrs7702192
googlers7702192
pharmgkbrs7702192
gwascentralrs7702192
openSNPrs7702192
23andMers7702192
23andMe allrs7702192
SNP Nexus

SNPshotrs7702192
SNPdbers7702192
MSV3drs7702192
GWAS Ctlgrs7702192
GMAF0.4624
Max Magnitude
? (A;A) (A;C) (C;C) 28

[PMID 22781450] [Association analysis of PDE8B gene polymorphisms with the susceptibility to Hyperthyroxinemia in Chinese Han population]