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rs655167

From SNPedia

Orientationminus
Stabilizedminus
Make rs655167(C;C)
Make rs655167(C;T)
Make rs655167(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position187933850
is asnp
is mentioned by
dbSNPrs655167
ebirs655167
HLIrs655167
Exacrs655167
Varsomers655167
Maprs655167
PheGenIrs655167
hapmaprs655167
1000 genomesrs655167
hgdprs655167
ensemblrs655167
gopubmedrs655167
geneviewrs655167
scholarrs655167
googlers655167
pharmgkbrs655167
gwascentralrs655167
openSNPrs655167
23andMers655167
23andMe allrs655167
SNP Nexus

SNPshotrs655167
SNPdbers655167
MSV3drs655167
GWAS Ctlgrs655167
GMAF0.1648
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22493691OA-icon.png]
Trait
Title Novel associations for hypothyroidism include known autoimmune risk loci.
Risk Allele A
P-val 0.000007
Odds Ratio 1.2590 None