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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
ebirs755109
HLIrs755109
Exacrs755109
Varsomers755109
Maprs755109
PheGenIrs755109
hapmaprs755109
1000 genomesrs755109
hgdprs755109
ensemblrs755109
gopubmedrs755109
geneviewrs755109
scholarrs755109
googlers755109
pharmgkbrs755109
gwascentralrs755109
openSNPrs755109
23andMers755109
23andMe allrs755109
SNP Nexus

SNPshotrs755109
SNPdbers755109
MSV3drs755109
GWAS Ctlgrs755109
GMAF0.2649
Max Magnitude
? (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.


GET Evidence
rs755109
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.296875
summary