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rs10848704

From SNPedia

Orientationplus
Stabilizedplus
Make rs10848704(C;C)
Make rs10848704(C;T)
Make rs10848704(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position2773378
GeneLOC283440
is asnp
is mentioned by
dbSNPrs10848704
ebirs10848704
HLIrs10848704
Exacrs10848704
Varsomers10848704
Maprs10848704
PheGenIrs10848704
hapmaprs10848704
1000 genomesrs10848704
hgdprs10848704
ensemblrs10848704
gopubmedrs10848704
geneviewrs10848704
scholarrs10848704
googlers10848704
pharmgkbrs10848704
gwascentralrs10848704
openSNPrs10848704
23andMers10848704
23andMe allrs10848704
SNP Nexus

SNPshotrs10848704
SNPdbers10848704
MSV3drs10848704
GWAS Ctlgrs10848704
GMAF0.2663
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 0.000002
Odds Ratio 0.29 [NR] mIU/L decrease

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


GET Evidence
rs10848704
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.693548
summary