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rs229526

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs229526(C;G)
Make rs229526(G;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position37185382
GeneC1QTNF6
is asnp
is mentioned by
dbSNPrs229526
ebirs229526
HLIrs229526
Exacrs229526
Varsomers229526
Maprs229526
PheGenIrs229526
hapmaprs229526
1000 genomesrs229526
hgdprs229526
ensemblrs229526
gopubmedrs229526
geneviewrs229526
scholarrs229526
googlers229526
pharmgkbrs229526
gwascentralrs229526
openSNPrs229526
23andMers229526
23andMe allrs229526
SNP Nexus

SNPshotrs229526
SNPdbers229526
MSV3drs229526
GWAS Ctlgrs229526
GMAF0.1804
Max Magnitude0
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 22493691OA-icon.png]
Trait
Title Novel associations for hypothyroidism include known autoimmune risk loci.
Risk Allele C
P-val 0.000009
Odds Ratio 1.2160 None


GET Evidence
C1QTNF6-P42R
aa_change Pro42Arg
aa_change_short P42R
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.239636
summary