Have questions? Visit https://www.reddit.com/r/SNPedia

rs3129720

From SNPedia

Orientationplus
Stabilizedplus
Make rs3129720(C;C)
Make rs3129720(C;T)
Make rs3129720(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position32695854
is asnp
is mentioned by
dbSNPrs3129720
ebirs3129720
HLIrs3129720
Exacrs3129720
Varsomers3129720
Maprs3129720
PheGenIrs3129720
hapmaprs3129720
1000 genomesrs3129720
hgdprs3129720
ensemblrs3129720
gopubmedrs3129720
geneviewrs3129720
scholarrs3129720
googlers3129720
pharmgkbrs3129720
gwascentralrs3129720
openSNPrs3129720
23andMers3129720
23andMe allrs3129720
SNP Nexus

SNPshotrs3129720
SNPdbers3129720
MSV3drs3129720
GWAS Ctlgrs3129720
GMAF0.2039
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 C
P-val 5E-7
Odds Ratio 1.1600 None
GWAS snp
PMID [PMID 23472185OA-icon.png]
Trait Multiple sclerosis (OCB status)
Title Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles.
Risk Allele
P-val 5E-15
Odds Ratio 1.91 [1.62-2.24]