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

rs9901756

From SNPedia

Orientationplus
Stabilizedplus
Make rs9901756(A;A)
Make rs9901756(A;C)
Make rs9901756(C;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position34137135
GeneASIC2
is asnp
is mentioned by
dbSNPrs9901756
ebirs9901756
HLIrs9901756
Exacrs9901756
Varsomers9901756
Maprs9901756
PheGenIrs9901756
hapmaprs9901756
1000 genomesrs9901756
hgdprs9901756
ensemblrs9901756
gopubmedrs9901756
geneviewrs9901756
scholarrs9901756
googlers9901756
pharmgkbrs9901756
gwascentralrs9901756
openSNPrs9901756
23andMers9901756
23andMe allrs9901756
SNP Nexus

SNPshotrs9901756
SNPdbers9901756
MSV3drs9901756
GWAS Ctlgrs9901756
GMAF0.1042
Max Magnitude
? (A;A) (A;C) (C;C) 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 1.2100 None