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rs6909430

From SNPedia

Orientationplus
Stabilizedplus
Make rs6909430(A;A)
Make rs6909430(A;G)
Make rs6909430(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position98291898
is asnp
is mentioned by
dbSNPrs6909430
ebirs6909430
HLIrs6909430
Exacrs6909430
Varsomers6909430
Maprs6909430
PheGenIrs6909430
hapmaprs6909430
1000 genomesrs6909430
hgdprs6909430
ensemblrs6909430
gopubmedrs6909430
geneviewrs6909430
scholarrs6909430
googlers6909430
pharmgkbrs6909430
gwascentralrs6909430
openSNPrs6909430
23andMers6909430
23andMe allrs6909430
SNP Nexus

SNPshotrs6909430
SNPdbers6909430
MSV3drs6909430
GWAS Ctlgrs6909430
GMAF0.1717
Max Magnitude
? (A;A) (A;G) (G;G) 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 G
P-val 0.000008
Odds Ratio 0.49 [NR] mIU/L decrease

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


GET Evidence
rs6909430
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.8125
summary