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rs755109

From SNPedia

Orientationplus
Stabilizedplus
Make rs755109(C;C)
Make rs755109(C;T)
Make rs755109(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position97933921
GeneHEMGN
is asnp
is mentioned by
dbSNPrs755109
dbSNP (classic)rs755109
ClinGenrs755109
ebirs755109
HLIrs755109
Exacrs755109
Gnomadrs755109
Varsomers755109
LitVarrs755109
Maprs755109
PheGenIrs755109
Biobankrs755109
1000 genomesrs755109
hgdprs755109
ensemblrs755109
geneviewrs755109
scholarrs755109
googlers755109
pharmgkbrs755109
gwascentralrs755109
openSNPrs755109
23andMers755109
SNPshotrs755109
SNPdbers755109
MSV3drs755109
GWAS Ctlgrs755109
GMAF0.2649
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 19197348OA-icon.png]
Trait Quantitative traits
Title Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae
Risk Allele C
P-val 0.000001
Odds Ratio 0.31 [NR] mIU/L decrease

Thyroid-stimulating hormone being the quantitative trait associated with in [PMID 19197348OA-icon.png]


[PMID 22493691OA-icon.png] Novel associations for hypothyroidism include known autoimmune risk loci.