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rs10499559

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs10499559(C;T)
Make rs10499559(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position22069841
is asnp
is mentioned by
dbSNPrs10499559
ebirs10499559
HLIrs10499559
Exacrs10499559
Varsomers10499559
Maprs10499559
PheGenIrs10499559
hapmaprs10499559
1000 genomesrs10499559
hgdprs10499559
ensemblrs10499559
gopubmedrs10499559
geneviewrs10499559
scholarrs10499559
googlers10499559
pharmgkbrs10499559
gwascentralrs10499559
openSNPrs10499559
23andMers10499559
23andMe allrs10499559
SNP Nexus

SNPshotrs10499559
SNPdbers10499559
MSV3drs10499559
GWAS Ctlgrs10499559
GMAF0.1703
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS
SNP rs10499559
PubMedID [PMID 17903292OA-icon.png]
Condition Thyroid stimulating hormone
Gene RAPGEF5
Risk Allele
pValue 8.00E-006
OR NA
95% CI



GET Evidence
rs10499559
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.164062
summary